Disease #04237 (DDOD (deafness-onychodystrophy, dominant (DDOD)), OMIM:124480)

Official abbreviation DDOD
Name deafness-onychodystrophy, dominant (DDOD)
OMIM ID 124480
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene ATP6V1B2
Associated tissues -
Disease features -
Remarks -
Date created 2015-04-04 22:00:53 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00037514 - PubMed: Yuan et al 2014 - F no China Asian - - - - DDOD - ATP6V1B2 ATP6V1B2 1 1 Philippe Campeau
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