ZFIN Human Disease: autosomal recessive nonsyndromic deafness 79

OBO ID: DOID:0110526

Term Name:	autosomal recessive nonsyndromic deafness 79		Search Ontology:
Synonyms:	autosomal recessive deafness 79 DFNB79
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 TPRN gene on chromosome 9q34. https://www.ncbi.nlm.nih.gov/pubmed/20170899
References:	ICD10CM:H90.3 OMIM:613307
Ontology:	Human Disease ( DOID:0110526 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 79 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TPRN	tprn	Deafness, autosomal recessive 79	613307

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None