ZFIN Human Disease: autosomal recessive nonsyndromic deafness 18B

OBO ID: DOID:0110474

Term Name:	autosomal recessive nonsyndromic deafness 18B		Search Ontology:
Synonyms:	autosomal recessive deafness 18B DFNB18B
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/23122587
References:	ICD10CM:H90.3 OMIM:614945
Ontology:	Human Disease ( DOID:0110474 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 18B PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OTOG	otog	Deafness, autosomal recessive 18B	614945

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None