ZFIN Human Disease: autosomal recessive nonsyndromic deafness 97

OBO ID: DOID:0110539

Term Name:	autosomal recessive nonsyndromic deafness 97		Search Ontology:
Synonyms:	autosomal recessive deafness 97 DFNB97
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MET gene on chromosome 7q31. https://www.ncbi.nlm.nih.gov/pubmed/25941349
References:	ICD10CM:H90.3 OMIM:616705
Ontology:	Human Disease ( DOID:0110539 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 97 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MET	met	?Deafness, autosomal recessive 97	616705

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None