ZFIN Human Disease: autosomal recessive nonsyndromic deafness 3

OBO ID: DOID:0110488

Term Name:	autosomal recessive nonsyndromic deafness 3		Search Ontology:
Synonyms:	autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3 DFNB3 NRSD3
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 MYO15A gene on chromosome 17p11. https://www.ncbi.nlm.nih.gov/pubmed/17851452
References:	ICD10CM:H90.3 OMIM:600316
Ontology:	Human Disease ( DOID:0110488 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 3 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYO15A	myo15ab myo15aa	Deafness, autosomal recessive 3	600316

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None