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autosomal recessive nonsyndromic deafness 35

Disease Summary
Associated Targets (1)
Tchem

1


Mondo Description Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the ESRRB gene.
Uniprot Description A form of non-syndromic deafness characterized by non-progressive, prelingual hearing loss.
Mondo Term and Equivalent IDs
MONDO:0012060:  autosomal recessive nonsyndromic deafness 35
MESH:C563908: 
UMLS:C1837857: