Disease #02397 (DFNA13 (deafness, autosomal dominant, type 13 (DFNA-13)), OMIM:601868)

Official abbreviation DFNA13
Name deafness, autosomal dominant, type 13 (DFNA-13)
OMIM ID 601868
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene COL11A2
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

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00043771 26306646-Pat#6 PubMed: Koolen 2016 - F - - - - - - - DFNA13, KDVS 17q21.31 deletion syndrome, see paper; … - - 1 1 David Koolen
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