Disease #01271 (CDHS (craniofacial deafness hand syndrome (CDHS)), OMIM:122880)

Official abbreviation CDHS
Name craniofacial deafness hand syndrome (CDHS)
OMIM ID 122880
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PAX3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00315519 - PubMed: Bolk 1996 - - - - - - - - - CDHS - EDN3 EDN3 1 1 Veronique Pingault
00315630 - PubMed: Asher 1996 - - - - - - - - - CDHS - PAX3 PAX3 1 1 Veronique Pingault
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