Disease #02810 (DFNB36 (deafness, autosomal recessive, type 36, with/without vestibular involvement (DFNB-36)), OMIM:609006)

Official abbreviation DFNB36
Name deafness, autosomal recessive, type 36, with/without vestibular involvement (DFNB-36)
OMIM ID 609006
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene ESPN
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)

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