Disease #02822 (Auditory neuropathy, autosomal dominant, 1, OMIM:609129)

Official abbreviation -
Name Auditory neuropathy, autosomal dominant, 1
OMIM ID 609129
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease 1
Associated with 1 gene DIAPH3
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.