Disease #02596 (DFNA36 (deafness, autosomal dominant, type 36 (DFNA-36)), OMIM:606705)

Official abbreviation DFNA36
Name deafness, autosomal dominant, type 36 (DFNA-36)
OMIM ID 606705
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene TMC1
Associated tissues -
Disease features -
Remarks -

  Powered by LOVD v.3.0 Build 28d
LOVD software ©2004-2023 Leiden University Medical Center 		There are currently no updates.