ZFIN Human Disease: autosomal recessive nonsyndromic deafness 1B

OBO ID: DOID:0110476

Term Name:	autosomal recessive nonsyndromic deafness 1B		Search Ontology:
Synonyms:	autosomal recessive deafness 1B DFNB1B
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/11807148
References:	ICD10CM:H90.3 OMIM:612645
Ontology:	Human Disease ( DOID:0110476 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 1B PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GJB2	gjb8	Deafness, autosomal recessive 1B	612645
GJB6	gjb8	Deafness, autosomal recessive 1B	612645

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None