View a developmental anomaly category

Developmental anomaly categoryinformation for Twin pathology

Description: (empty)


Developmental anomalies associated with this developmental anomaly category :

Array
(
    [Dacategory] => Array
        (
            [id] => 31
            [name] => Twin pathology
            [description] => 
        )

    [Thesaurus] => Array
        (
            [0] => Array
                (
                    [id] => 278
                    [name] => Acardiac twinning, with pump twin demise
                    [description] => The acardiac monster is the most extreme manifestation of the feto-fetal transfusion syndrome. Most of the acardiac monsters have been reported in monochorionic twins (98%).
                    [author_id] => 1
                    [topo_code] => 1
                    [category_code] => 31
                    [system_code] => 1
                    [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] => 2008-05-27 02:00:00
                    [modified] => 2009-01-06 22:09:18
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [1] => Array
                (
                    [id] => 318
                    [name] => Conjoined twins
                    [description] => Conjoined twins are identical twins whose bodies are joined in utero.About 70% to 75% of conjoined twin pairs are female.
                    [author_id] => 1
                    [topo_code] => 0
                    [category_code] => 31
                    [system_code] => 0
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 
                    [omim_ref] => 
                    [possum_ref] => 
                    [snomed_ref] => 
                    [ICD10_ref] => Q89.4
                    [orphanet_ref] => 
                    [emedicine_ref] => 
                    [diseasesdb_ref] => 
                    [mesh_ref] => 
                    [fetusnet_ref] => 
                    [wiki_ref] => 
                    [created] => 2008-06-02 02:00:00
                    [modified] => 2009-01-05 17:30:38
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

            [2] => Array
                (
                    [id] => 488
                    [name] => Complete hydatidiform mole with a coexistent embryo
                    [description] => 
                    [author_id] => 3
                    [topo_code] => 0
                    [category_code] => 31
                    [system_code] => 0
                    [parent_da_code] => 73
                    [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] => 2008-08-05 21:50:59
                    [modified] => 2009-01-05 16:12:02
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                )

        )

)