ZFIN Human Disease: autosomal recessive nonsyndromic deafness 37

OBO ID: DOID:0110495

Term Name:	autosomal recessive nonsyndromic deafness 37		Search Ontology:
Synonyms:	autosomal recessive deafness 37 DFNB37
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/12687499
References:	ICD10CM:H90.3 OMIM:607821
Ontology:	Human Disease ( DOID:0110495 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 37 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYO6	myo6b myo6a	Deafness, autosomal recessive 37	607821

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None