ZFIN Human Disease: autosomal recessive nonsyndromic deafness 39

OBO ID: DOID:0110497

Term Name:	autosomal recessive nonsyndromic deafness 39		Search Ontology:
Synonyms:	autosomal recessive deafness 39 DFNB39
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/19576567
References:	ICD10CM:H90.3 OMIM:608265
Ontology:	Human Disease ( DOID:0110497 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 39 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
HGF	hgfa hgfb	Deafness, autosomal recessive 39	608265

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None