ZFIN Human Disease: autosomal recessive nonsyndromic deafness 91

OBO ID: DOID:0110536

Term Name:	autosomal recessive nonsyndromic deafness 91		Search Ontology:
Synonyms:	autosomal recessive deafness 91 DFNB91
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SERPINB6 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/20451170
References:	ICD10CM:H90.3 OMIM:613453
Ontology:	Human Disease ( DOID:0110536 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 91 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SERPINB6		?Deafness, autosomal recessive 91

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None