ZFIN Human Disease: autosomal recessive nonsyndromic deafness 110

OBO ID: DOID:0111644

Term Name:	autosomal recessive nonsyndromic deafness 110		Search Ontology:
Synonyms:	autosomal recessive deafness 110 DFNB110
Definition:	An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/29449721
References:	OMIM:618094
Ontology:	Human Disease ( DOID:0111644 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 110 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
COCH	coch	?Deafness, autosomal recessive 110	618094

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None