ZFIN Human Disease: autosomal recessive nonsyndromic deafness 2

OBO ID: DOID:0110477

Term Name:	autosomal recessive nonsyndromic deafness 2		Search Ontology:
Synonyms:	autosomal recessive deafness 2 DFNB2
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/9171833
References:	ICD10CM:H90.3 OMIM:600060
Ontology:	Human Disease ( DOID:0110477 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 2 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYO7A	myo7ab myo7aa	Deafness, autosomal recessive 2	600060

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None