View a developmental anomaly category

Developmental anomaly categoryinformation for Agenesis

Description: Absence of part of body caused by an absent analge (primordium).


Developmental anomalies associated with this developmental anomaly category :

Array
(
    [Dacategory] => Array
        (
            [id] => 14
            [name] => Agenesis
            [description] => Absence  of part of body caused by an absent analge (primordium).
        )

    [Thesaurus] => Array
        (
            [0] => Array
                (
                    [id] => 811
                    [name] => Thumb agenesis
                    [description] => Aplasia or hypoplasia of the thumb is often associated with other malformations. These include anomalies of the carpus, club hand due to aplasia or hypoplasia of the radius, radioulnar synostosis, Fanconi's anaemia and Holt-Oram syndrome. Thalidomide caused an increased incidence
                    [author_id] => 3
                    [topo_code] => 77
                    [category_code] => 14
                    [system_code] => 9
                    [parent_da_code] => 813
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-12-17 19:27:37
                    [modified] => 2009-01-06 18:46:40
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [1] => Array
                (
                    [id] => 71
                    [name] => Renal agenesis, bilateral
                    [description] => Bilateral Renal Agenesis is the absence of both kidneys at birth characterized by a failure of the kidneys to develop in a fetus. The kidneys develop between the 5th and 12th week of fetal life, and by the 13th week they are normally producing urine. 
                    [author_id] => 1
                    [topo_code] => 41
                    [category_code] => 14
                    [system_code] => 32
                    [parent_da_code] => 833
                    [adicap_ref] => 
                    [humpath_ref] => 2412
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q60.1
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-02-26 00:00:00
                    [modified] => 2008-12-19 19:11:30
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [2] => Array
                (
                    [id] => 72
                    [name] => Agenesia of internal genital organs
                    [description] => Absence of differentiation/regression of the internal ducts (ie, müllerian and wolffian ducts) which ultimately determines the phenotypic sex. 
                    [author_id] => 1
                    [topo_code] => 18
                    [category_code] => 14
                    [system_code] => 56
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 13369
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-02-26 00:00:00
                    [modified] => 2009-01-07 16:35:51
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [3] => Array
                (
                    [id] => 105
                    [name] => Renal agenesis, unilateral
                    [description] => 
                    [author_id] => 1
                    [topo_code] => 41
                    [category_code] => 14
                    [system_code] => 32
                    [parent_da_code] => 833
                    [adicap_ref] => 
                    [humpath_ref] => 5618
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q60.0 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-03-07 00:00:00
                    [modified] => 2008-12-19 19:08:40
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [4] => Array
                (
                    [id] => 169
                    [name] => Thumb agenesis, bilateral
                    [description] => The thumb is absent bilaterally.
                    [author_id] => 1
                    [topo_code] => 77
                    [category_code] => 14
                    [system_code] => 9
                    [parent_da_code] => 811
                    [adicap_ref] => 
                    [humpath_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-05-09 00:00:00
                    [modified] => 2008-12-17 19:36:23
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [5] => Array
                (
                    [id] => 183
                    [name] => Absence of diaphragm, left
                    [description] =>  Congenital absence of the diaphragm is a rare condition where part or all of the diaphragm missing.The thoracic diaphragm is a sheet of muscle extending across the bottom of the ribcage. The diaphragm separates the thoracic cavity from the abdominal cavity and performs an important function in respiration




                    [author_id] => 1
                    [topo_code] => 3
                    [category_code] => 14
                    [system_code] => 43
                    [parent_da_code] => 582
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q79.1 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-12 00:00:00
                    [modified] => 2009-01-06 16:57:40
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [6] => Array
                (
                    [id] => 187
                    [name] => Thumb agenesis, unilateral
                    [description] => 
                    [author_id] => 1
                    [topo_code] => 34
                    [category_code] => 14
                    [system_code] => 9
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 4142
                    [omim_ref] => 
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                    [ICD10_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-05-12 00:00:00
                    [modified] => 2008-12-04 13:40:27
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [7] => Array
                (
                    [id] => 190
                    [name] => Ureter agenesis, bilateral
                    [description] => Congenital absence of ureter. It is usually associated with a renal agenesis.
                    [author_id] => 1
                    [topo_code] => 43
                    [category_code] => 14
                    [system_code] => 33
                    [parent_da_code] => 757
                    [adicap_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-05-12 00:00:00
                    [modified] => 2009-01-07 15:46:42
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [8] => Array
                (
                    [id] => 191
                    [name] => Uterus agenesis
                    [description] => Absence of the Uterus (Vaginal Agenesis) is when the uterus and upper vagina do not form properly. Abnormalities of the kidneys or bones may occur as well.
                    [author_id] => 1
                    [topo_code] => 20
                    [category_code] => 14
                    [system_code] => 41
                    [parent_da_code] => 864
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q51.0 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-12 00:00:00
                    [modified] => 2009-01-06 20:58:10
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [9] => Array
                (
                    [id] => 192
                    [name] => Fallopian tube, absence of
                    [description] => Congenital müllerian duct abnormalities are considered fairly common and have been estimated to be present in 1 in 500–700 females.  The complete unilateral absence of a fallopian tube is a very rare condition that is usually entirely asymptomatic.
                    [author_id] => 1
                    [topo_code] => 20
                    [category_code] => 14
                    [system_code] => 40
                    [parent_da_code] => 864
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q50.6 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-12 00:00:00
                    [modified] => 2009-01-06 17:20:58
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [10] => Array
                (
                    [id] => 201
                    [name] => Absence of the Septum Pellucidum
                    [description] => Absence of the septum pellucidum can be associated with septooptic dysplasia; schizencephaly; holoprosencephaly; agenesis of the corpus callosum; chronic, severe hydrocephalus; basilar encephaloceles; and porencephaly/hydranencephaly.

                    [author_id] => 1
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
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                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-13 00:00:00
                    [modified] => 2008-12-02 14:25:26
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [11] => Array
                (
                    [id] => 234
                    [name] => Anotia
                    [description] => Anotia is the absence of the external ear, the auricle and/or the visible part of the ear.
                    [author_id] => 1
                    [topo_code] => 59
                    [category_code] => 14
                    [system_code] => 53
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q16.0 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-16 00:00:00
                    [modified] => 2008-12-17 15:55:15
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [12] => Array
                (
                    [id] => 272
                    [name] => Clivus, absence of
                    [description] => Clivus is a downward sloping surface. The sloping surface from the dorsum sellae to the foramen magnum composed of part of the body of the sphenoid and part of the basal part of the occipital bone.
                    [author_id] => 1
                    [topo_code] => 46
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-26 00:00:00
                    [modified] => 2009-01-06 16:04:18
                    [modified_by] => 2
                    [test] => 0
                    [isFree] => 0
                )

            [13] => Array
                (
                    [id] => 276
                    [name] => Acardia
                    [description] => Acardia is a very rare, serious malformation that occurs almost exclusively in monozygous twins .Acardia is the most extreme form of twin-twin transfusion syndrome
                    [author_id] => 1
                    [topo_code] => 11
                    [category_code] => 14
                    [system_code] => 46
                    [parent_da_code] => 278
                    [adicap_ref] => 
                    [humpath_ref] => 
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                    [ICD10_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-05-26 00:00:00
                    [modified] => 2009-01-06 21:07:34
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [14] => Array
                (
                    [id] => 280
                    [name] => Absence of one paire the rib
                    [description] => It is more common to see 11 pairs in the absence of associated anomalies; this situation occurs in 5%–8% of normal individuals. Eleven pairs of ribs occur in one-third of patients with trisomy 21 syndrome , as well as in association with cleidocranial dysplasia and campomelic dysplasia. 



                    [author_id] => 1
                    [topo_code] => 3
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q76.6
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-27 00:00:00
                    [modified] => 2009-01-06 20:29:28
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [15] => Array
                (
                    [id] => 281
                    [name] => Clavicle, absence of
                    [description] =>  Absence of clavicle is usually associated with other fetal anomalies, like Cleidocranial dysplasia (CCD).
                    [author_id] => 1
                    [topo_code] => 3
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
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                    [ICD10_ref] => 
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                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-27 00:00:00
                    [modified] => 2009-01-06 17:16:11
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [16] => Array
                (
                    [id] => 290
                    [name] => Ureter agenesis, unilateral
                    [description] => 
                    [author_id] => 1
                    [topo_code] => 43
                    [category_code] => 14
                    [system_code] => 33
                    [parent_da_code] => 757
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-29 00:00:00
                    [modified] => 2009-01-07 15:45:56
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [17] => Array
                (
                    [id] => 293
                    [name] => Frontal Bone Agenesis
                    [description] => A cranial abnormality associated with other facial dysmorphisms
                    [author_id] => 1
                    [topo_code] => 46
                    [category_code] => 14
                    [system_code] => 50
                    [parent_da_code] => 506
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-29 00:00:00
                    [modified] => 2008-12-31 18:06:23
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [18] => Array
                (
                    [id] => 305
                    [name] => Lumbosacral agenesis
                    [description] => Caudal Regression Syndrome is a rare disorder involves absence of the sacrococcygeal vertebrae with or without lumbar vertebral defects.
                    [author_id] => 1
                    [topo_code] => 68
                    [category_code] => 14
                    [system_code] => 9
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 10649
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-29 00:00:00
                    [modified] => 2008-12-16 19:41:06
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [19] => Array
                (
                    [id] => 314
                    [name] => Corpus callosum agenesis
                    [description] => ACC is the failure of formation or decussation of the corticocortical fibers. ACC may be an isolated feature or associated with other malformations.
                    [author_id] => 1
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 509
                    [adicap_ref] => 
                    [humpath_ref] => 40
                    [omim_ref] => 	217990
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q04.0
                    [orphanet_ref] => 
                    [emedicine_ref] => 	radio/193
                    [diseasesdb_ref] => 	29900
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-30 00:00:00
                    [modified] => 2009-01-06 17:07:28
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [20] => Array
                (
                    [id] => 315
                    [name] => Partial agenesis of the corpus callosum (PACC)
                    [description] => In partial agenesis of the corpus callosum, the body and the splenium are usually absent
                    [author_id] => 1
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 314
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
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                    [ICD10_ref] => 
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                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-05-30 00:00:00
                    [modified] => 2008-12-19 22:28:12
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [21] => Array
                (
                    [id] => 343
                    [name] => Femur agenesis, unilateral
                    [description] => associated with femoral facial syndrome 
                    [author_id] => 1
                    [topo_code] => 23
                    [category_code] => 14
                    [system_code] => 9
                    [parent_da_code] => 126
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q72.4
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-06-03 00:00:00
                    [modified] => 2008-12-30 14:45:17
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [22] => Array
                (
                    [id] => 353
                    [name] => Absence of neocortex
                    [description] => definition of the Neocortex:The neocortex  is the outer layer of the cerebral hemispheres, and made up of six layers, labelled I to VI (with VI being the innermost and I being the outermost). The neocortex is part of the cerebral cortex (along with the archicortex and paleocortex, which are cortical parts of the limbic system). It is involved in higher functions such as sensory perception, generation of motor commands, spatial reasoning, conscious thought and, in humans, language. Other names for the neocortex include neopallium ("new mantel") and isocortex ("equal rind").



                    [author_id] => 1
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-06-03 00:00:00
                    [modified] => 2009-01-06 20:02:09
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [23] => Array
                (
                    [id] => 354
                    [name] => Absence of the pyramid tracts, bilateral
                    [description] => Absence of the pyramids  observed in  X-linked congenital aqueduct stenosis, non X-linked congenital microcephaly and also several known or new genetic syndromes eg: Meckel's syndrome.  
                    [author_id] => 1
                    [topo_code] => 63
                    [category_code] => 14
                    [system_code] => 14
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-06-03 00:00:00
                    [modified] => 2008-12-02 15:06:22
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [24] => Array
                (
                    [id] => 366
                    [name] => Lung agenesis, unilateral
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 9
                    [category_code] => 14
                    [system_code] => 20
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q33.3 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-06-09 16:36:06
                    [modified] => 2008-12-16 17:13:44
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [25] => Array
                (
                    [id] => 422
                    [name] => Absence of innominate (brachiocephalic) vein
                    [description] => Brachiocephalic vein definition:
The left and right brachiocephalic veins (or innominate veins) in the upper chest are formed by the union of each corresponding internal jugular vein and subclavian vein.

These great vessels merge to form the superior vena cava.

The brachiocephalic veins are the major veins returning blood to the superior vena cava.

                    [author_id] => 3
                    [topo_code] => 52
                    [category_code] => 14
                    [system_code] => 49
                    [parent_da_code] => 0
                    [adicap_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-06-20 18:21:59
                    [modified] => 2009-01-06 19:32:24
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [26] => Array
                (
                    [id] => 778
                    [name] => Cerebellar vermis agenesis
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 62
                    [category_code] => 14
                    [system_code] => 13
                    [parent_da_code] => 202
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-22 18:06:31
                    [modified] => 2009-01-07 15:16:45
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [27] => Array
                (
                    [id] => 446
                    [name] => Olfactory bulbs, absence of
                    [description] => Absence of  olfactory bulbs is when the olfactory nerves does not make contact with the brain.The presence of olfactory nerves is independent of the severity of the central nervous system malformation, and  the shape of the nasal sturctures is not dependent on the presence of the olfactory nerve. 
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 268
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
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                    [diseasesdb_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-07-21 23:01:16
                    [modified] => 2009-01-07 17:32:39
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [28] => Array
                (
                    [id] => 447
                    [name] => Sacrococcygeal agenesis
                    [description] => Sacrococcygeal agenesis is an uncommon condition (about 200 cases are recorded in the medical literature) affecting the normal development of sacrum and coccyx.
                    [author_id] => 2
                    [topo_code] => 0
                    [category_code] => 14
                    [system_code] => 0
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
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                    [mesh_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-07-23 14:22:13
                    [modified] => 2008-12-02 16:12:20
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [29] => Array
                (
                    [id] => 499
                    [name] => Olfactory nerve, absence of, unilateral
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 805
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-06 14:49:35
                    [modified] => 2009-01-06 20:21:58
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [30] => Array
                (
                    [id] => 508
                    [name] => Absence of hippocampal commissure
                    [description] => usually associated with Agenesis of the Corpus Callosum
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 509
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
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                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-06 19:12:51
                    [modified] => 2009-01-06 19:30:41
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [31] => Array
                (
                    [id] => 509
                    [name] => Cerebral commissures agenesis
                    [description] => The cerebral commissures house the fibers that interconnect the two hemispheres of the brain. The main fiber tract, namely the corpus callosum, varies greatly in size in the human brain. 
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
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                    [diseasesdb_ref] => 
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                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-06 21:16:59
                    [modified] => 2009-01-07 15:20:20
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [32] => Array
                (
                    [id] => 710
                    [name] => absence of nasal septum
                    [description] => Congenital anomalies of the nasal septum, except septal deviation, constitute a small portion of all congenital nasal anomalies. Congenital septal anomalies are extremely rare.
                    [author_id] => 3
                    [topo_code] => 74
                    [category_code] => 14
                    [system_code] => 63
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-09-18 18:31:55
                    [modified] => 2009-01-06 19:52:02
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [33] => Array
                (
                    [id] => 669
                    [name] => Absence of skull bones
                    [description] => In humans, the adult skull is normally made up of 22 bones. Except for the mandible, all of the bones of the skull are joined together by sutures, rigid articulations permitting very little movement. Eight bones form the neurocranium (braincase)—including the frontal, parietals, occipital bone, sphenoid, temporals and ethmoid—a protective vault surrounding the brain. Fourteen bones form the splanchnocranium, the bones supporting the face. Encased within the temporal bones are the six ear ossicles of the middle ears, though these are not part of the skull. The hyoid bone, supporting the tongue, is usually not considered as part of the skull either, as it does not articulate with any other bones. The skull is a protector of the brain.

Agenesis of the cranial bones, a rare condition which defined as the absence of neurocranium (braincase).
                    [author_id] => 3
                    [topo_code] => 46
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
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                    [wiki_ref] => 
                    [created] => 2008-09-04 20:06:16
                    [modified] => 2009-01-07 14:22:24
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [34] => Array
                (
                    [id] => 529
                    [name] => Corticospinal tract absence
                    [description] => The corticospinal or pyramidal tract is a massive collection of axons that travel between the cerebral cortex of the brain and the spinal cord.


                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 50
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
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                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-08 13:19:01
                    [modified] => 2008-12-15 15:13:41
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [35] => Array
                (
                    [id] => 575
                    [name] => Absence of Cajal-Retzius cell
                    [description] => The term Cajal–Retzius cell is applied to reelin-producing neurons of the human embryonic marginal zone which display, as a salient feature, radial ascending processes that contact the pial surface, and a horizontal axon plexus located in the deep marginal zone.Cajal–Retzius cells produce  reelin, pointing to the spatiotemporal control of reelin expression as a key feature of cortical evolution.
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 50
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-19 12:58:10
                    [modified] => 2009-01-06 17:00:30
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [36] => Array
                (
                    [id] => 641
                    [name] => Anorchia, unilateral
                    [description] => 

                    [author_id] => 3
                    [topo_code] => 80
                    [category_code] => 14
                    [system_code] => 36
                    [parent_da_code] => 881
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q55.0 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-27 20:43:46
                    [modified] => 2009-01-07 17:21:54
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [37] => Array
                (
                    [id] => 653
                    [name] => Bladder agenesis
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 19
                    [category_code] => 14
                    [system_code] => 34
                    [parent_da_code] => 857
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-08-29 19:32:32
                    [modified] => 2009-01-05 20:43:19
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [38] => Array
                (
                    [id] => 684
                    [name] => Olfactory nerve, absence of, bilateral
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 805
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-09-10 13:33:54
                    [modified] => 2009-01-06 20:20:43
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [39] => Array
                (
                    [id] => 732
                    [name] => Agenesis of ribs, partial
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 8
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 838
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-01 12:37:19
                    [modified] => 2008-12-19 22:25:15
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [40] => Array
                (
                    [id] => 754
                    [name] => Holoanencephaly
                    [description] => Holoanencephaly is the most common type of anencephaly, in which the brain is completely absent.
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-16 12:59:12
                    [modified] => 2008-12-15 16:54:17
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [41] => Array
                (
                    [id] => 757
                    [name] => Ureter agenesis
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 43
                    [category_code] => 14
                    [system_code] => 33
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-16 18:02:52
                    [modified] => 2009-01-07 15:50:14
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [42] => Array
                (
                    [id] => 784
                    [name] => Absence of Anterior Commissure
                    [description] => The Anterior Commissure (precommissure) is a bundle of white fibers, connecting the two cerebral hemispheres across the middle line, and placed in front of the columns of the fornix.On a sagittal section, it is oval in shape, having a long vertical diameter that measures about 5 mm.
Its fibers can be traced laterally and backwards on either side beneath the corpus striatum into the substance of the temporal lobe.

It serves in this way to connect the two temporal lobes, but it also contains decussating fibers from the olfactory tracts, and is a part of the neospinothalamic tract for pain. The anterior commissure also serves to connect the two amygdala


                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 509
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
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                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-24 13:47:47
                    [modified] => 2009-01-06 19:46:19
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [43] => Array
                (
                    [id] => 785
                    [name] => Absence of Posterior Commissure
                    [description] => The posterior commissure is a rounded band of white fibers crossing the middle line on the dorsal aspect of the upper end of the cerebral aqueduct. It is important in the bilateral pupillary light reflex.
Its fibers acquire their medullary sheaths early, but their connections have not been definitely determined. Most of them have their origin in a nucleus, the nucleus of the posterior commissure (nucleus of Darkschewitsch), which lies in the central gray substance of the upper end of the cerebral aqueduct, in front of the nucleus of the oculomotor nerve.
Some are probably derived from the posterior part of the thalamus and from the superior colliculus, whereas others are believed to be continued downward into the medial longitudinal fasciculus.
The posterior commissure interconnects the pretectal nuclei, mediating the consensual pupillary light reflex.


                    [author_id] => 3
                    [topo_code] => 0
                    [category_code] => 14
                    [system_code] => 0
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-24 13:52:38
                    [modified] => 2008-12-02 14:59:12
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [44] => Array
                (
                    [id] => 791
                    [name] => Radial ray agenesis, unilateral
                    [description] => 
                    [author_id] => 2
                    [topo_code] => 31
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 814
                    [adicap_ref] => 
                    [humpath_ref] => 6237
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 3025
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-10-28 14:57:40
                    [modified] => 2008-12-17 20:21:08
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [45] => Array
                (
                    [id] => 800
                    [name] => Radial ray agenesis, bilateral
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 31
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 814
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-11-04 15:58:11
                    [modified] => 2008-12-17 20:18:47
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [46] => Array
                (
                    [id] => 805
                    [name] => Olfactory nerve, absence of
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 61
                    [category_code] => 14
                    [system_code] => 12
                    [parent_da_code] => 268
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-11-05 15:53:48
                    [modified] => 2009-01-07 17:35:41
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [47] => Array
                (
                    [id] => 814
                    [name] => Radial ray agenesis
                    [description] => Radial ray agenesis is a rare malformation manifested by the absence of radius with absence of the thumb column (scaphoid bone, 1st metacarpal, and thumb phalanges). This absence may be total or partial. It is normally associated with bowed ulna. Radial ray agenesis may be uni- or bilateral, isolated or associated with other defects. Radial ray agenesis is a sign included in several genetic syndromes, the least rare being thrombocytopenia and absent radii (TAR) syndrome, Roberts syndrome, Holt-Oram syndrome, and some chromosomal anomalies (ring of chromosome 4, or 4q deletion). It also is part of the association of malformations known as VATER (vertebral defects, anal atresia, tracheoesophageal fistula with esophageal atresia, and radial and renal anomalies). 
                    [author_id] => 3
                    [topo_code] => 31
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-12-17 20:15:31
                    [modified] => 2009-01-06 18:44:41
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [48] => Array
                (
                    [id] => 833
                    [name] => Renal agenesis
                    [description] => Renal agenesis can occur uni- or bilaterally, isolated or combined with other abnormalities 
                    [author_id] => 3
                    [topo_code] => 41
                    [category_code] => 14
                    [system_code] => 32
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-12-19 19:05:24
                    [modified] => 2008-12-19 19:05:24
                    [modified_by] => 
                    [test] => 0
                    [isFree] => 0
                )

            [49] => Array
                (
                    [id] => 838
                    [name] => ribs agenesis,
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 9
                    [category_code] => 14
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-12-19 22:19:41
                    [modified] => 2008-12-19 22:21:27
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [50] => Array
                (
                    [id] => 881
                    [name] => Anorchia
                    [description] => Absence of one or both testes 

                    [author_id] => 3
                    [topo_code] => 80
                    [category_code] => 14
                    [system_code] => 36
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => 
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2009-01-07 17:19:38
                    [modified] => 2009-01-07 17:21:35
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

        )

)