Visualize Submit Comment

Metadata
ID	DOID:0110493
Name	autosomal recessive nonsyndromic deafness 35
Definition	An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24. https://www.ncbi.nlm.nih.gov/pubmed/18179891
Xrefs	ICD10CM:H90.3 MIM:608565
Synonyms	autosomal recessive deafness 35 [EXACT] DFNB35 [EXACT]
Parent Relationships	is_a autosomal recessive nonsyndromic deafness