ZFIN Human Disease: autosomal recessive nonsyndromic deafness 77

OBO ID: DOID:0110525

Term Name:	autosomal recessive nonsyndromic deafness 77		Search Ontology:
Synonyms:	autosomal recessive deafness 77 DFNB77
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by postlingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the LOXHD1 gene on chromosome 18q21. https://www.ncbi.nlm.nih.gov/pubmed/19732867
References:	ICD10CM:H90.3 OMIM:613079
Ontology:	Human Disease ( DOID:0110525 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 77 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LOXHD1	loxhd1a loxhd1b	Deafness, autosomal recessive 77	613079

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None