ZFIN Human Disease: autosomal recessive nonsyndromic deafness 67

OBO ID: DOID:0110518

Term Name:	autosomal recessive nonsyndromic deafness 67		Search Ontology:
Synonyms:	autosomal recessive deafness 67 DFNB67
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 LHFPL5 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/16459341
References:	ICD10CM:H90.3 OMIM:610265
Ontology:	Human Disease ( DOID:0110518 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 67 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
LHFPL5	lhfpl5a lhfpl5b	Deafness, autosomal recessive 67	610265

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None