del(10)(p12p14) disease

DIS: 27




del(10)(p12p14) disease

Definition: (empty)


Synonyms:

  • del(10)(p12p14) syndrome

Category: (empty)

Developmental anomalies

Listed in the disease's profile :

Observed in MDB cases: (graph view)


There are no developmental anomalies for this disease.
Case records

Associated signaling pathways
Associations
Array
(
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        (
            [id] => 27
            [name] => del(10)(p12p14) disease
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                    [id] => 12
                    [disease_id] => 27
                    [name] => del(10)(p12p14) syndrome
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    [DAs] => Array
        (
            [0] => Array
                (
                    [id] => 46
                    [name] => Hypertelorism
                    [description] => Excessive width between two bodily parts or organs (as the eyes). Excessive orbital separation. HPO:0000316
                    [author_id] => 1
                    [topo_code] => 50
                    [category_code] => 7
                    [system_code] => 51
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 4553
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                    [created] => 2008-02-25 01:00:00
                    [modified] => 2009-05-05 16:50:43
                    [modified_by] => 2
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 35
                            [disease_id] => 27
                            [anomaly_id] => 46
                        )

                )

            [1] => Array
                (
                    [id] => 39
                    [name] => Microretrognathia
                    [description] => Anomalies of jaw-cranial base relationship
                    [author_id] => 1
                    [topo_code] => 48
                    [category_code] => 9
                    [system_code] => 44
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 13340
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                    [created] => 2008-02-22 01:00:00
                    [modified] => 2008-12-05 18:12:20
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
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                            [id] => 36
                            [disease_id] => 27
                            [anomaly_id] => 39
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            [2] => Array
                (
                    [id] => 317
                    [name] => Epicanthus
                    [description] => An epicanthal fold is skin of the upper eyelid, from the nose to the inner side of the eyebrow, that covers the inner corner (canthus) of the eye.
                    [author_id] => 1
                    [topo_code] => 50
                    [category_code] => 9
                    [system_code] => 51
                    [parent_da_code] => 55
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                    [created] => 2008-06-02 02:00:00
                    [modified] => 2008-12-16 17:43:18
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
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                            [id] => 37
                            [disease_id] => 27
                            [anomaly_id] => 317
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            [3] => Array
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                    [id] => 52
                    [name] => Broad nasal bridge
                    [description] => Broad nasal bridge is a widening of the top part of the nose, it can be associated with certain genetic or congenital disorders
                    [author_id] => 1
                    [topo_code] => 74
                    [category_code] => 9
                    [system_code] => 63
                    [parent_da_code] => 0
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                    [created] => 2008-02-25 01:00:00
                    [modified] => 2008-12-17 17:51:56
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 38
                            [disease_id] => 27
                            [anomaly_id] => 52
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            [4] => Array
                (
                    [id] => 296
                    [name] => Syndactyly, simple (webbed), fingers
                    [description] => 
                    [author_id] => 1
                    [topo_code] => 34
                    [category_code] => 9
                    [system_code] => 9
                    [parent_da_code] => 719
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                    [created] => 2008-05-29 02:00:00
                    [modified] => 2008-12-19 18:41:02
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
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                            [id] => 39
                            [disease_id] => 27
                            [anomaly_id] => 296
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            [5] => Array
                (
                    [id] => 55
                    [name] => Facial dysmorphism
                    [description] => Dysmorphisms of the fetal face are abnormalities in facial features which are usually associated with syndromic conditions.
                    [author_id] => 1
                    [topo_code] => 47
                    [category_code] => 9
                    [system_code] => 1
                    [parent_da_code] => 0
                    [adicap_ref] => 
                    [humpath_ref] => 3476
                    [omim_ref] => 
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                    [ICD10_ref] => Q75.9
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                    [created] => 2008-02-25 01:00:00
                    [modified] => 2008-12-11 20:32:17
                    [modified_by] => 3
                    [test] => 0
                    [isFree] => 0
                    [DiseasesAnomaly] => Array
                        (
                            [id] => 69
                            [disease_id] => 27
                            [anomaly_id] => 55
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    [SignalingPathways] => Array
        (
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)
Links

Humpath: (empty)

thefetus.net: (empty)

eMedicine: (empty)

OMIM: (empty)

Wikipedia: (empty)

DiseaseDB: (empty)