ZFIN Human Disease: autosomal recessive nonsyndromic deafness 18A

OBO ID: DOID:0110473

Term Name:	autosomal recessive nonsyndromic deafness 18A		Search Ontology:
Synonyms:	autosomal recessive deafness 18A DFNB18A
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the USH1C gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/12136232
References:	ICD10CM:H90.3 OMIM:602092
Ontology:	Human Disease ( DOID:0110473 )

Relationships

is a type of:	autosomal recessive nonsyndromic deafness autosomal recessive nonsyndromic deafness Show first 5 Terms

OTHER autosomal recessive nonsyndromic deafness 18A PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
USH1C	ush1c	Deafness, autosomal recessive 18A	602092

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None