ZFIN Human Disease: autosomal recessive nonsyndromic deafness 42

OBO ID: DOID:0110500

Term Name:	autosomal recessive nonsyndromic deafness 42		Search Ontology:
Synonyms:	autosomal recessive deafness 42 DFNB42
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ILDR1 gene on chromosome 3q13. https://www.ncbi.nlm.nih.gov/pubmed/21255762
References:	ICD10CM:H90.3 OMIM:609646
Ontology:	Human Disease ( DOID:0110500 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 42 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ILDR1	ildr1b ildr1a	Deafness, autosomal recessive 42	609646

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None