ZFIN Human Disease: autosomal recessive nonsyndromic deafness 7

OBO ID: DOID:0110520

Term Name:	autosomal recessive nonsyndromic deafness 7		Search Ontology:
Synonyms:	autosomal recessive deafness 7 DFNB11 DFNB7
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 TMC1 gene on chromosome 9q21. https://www.ncbi.nlm.nih.gov/pubmed/11850618
References:	ICD10CM:H90.3 OMIM:600974
Ontology:	Human Disease ( DOID:0110520 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 7 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TMC1	tmc1	Deafness, autosomal recessive 7	600974

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None