ZFIN Human Disease: autosomal recessive nonsyndromic deafness 103

OBO ID: DOID:0110464

Term Name:	autosomal recessive nonsyndromic deafness 103		Search Ontology:
Synonyms:	autosomal recessive deafness 103 DFNB103
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CLIC5 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/24781754
References:	ICD10CM:H90.3 OMIM:616042
Ontology:	Human Disease ( DOID:0110464 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 103 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CLIC5	clic5b clic5a	?Deafness, autosomal recessive 103	616042

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None