ZFIN Human Disease: autosomal recessive nonsyndromic deafness 6

OBO ID: DOID:0110512

Term Name:	autosomal recessive nonsyndromic deafness 6		Search Ontology:
Synonyms:	autosomal recessive deafness 6 DFNB6
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 TMIE gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/12145746
References:	ICD10CM:H90.3 OMIM:600971
Ontology:	Human Disease ( DOID:0110512 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 6 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TMIE	tmie	Deafness, autosomal recessive 6	600971

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None