ZFIN Human Disease: autosomal recessive nonsyndromic deafness 68

OBO ID: DOID:0110519

Term Name:	autosomal recessive nonsyndromic deafness 68		Search Ontology:
Synonyms:	autosomal recessive deafness 68 DFNB68
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the S1PR2 gene on chromosome 19p13. https://www.ncbi.nlm.nih.gov/pubmed/26805784
References:	ICD10CM:H90.3 OMIM:610419
Ontology:	Human Disease ( DOID:0110519 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 68 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
S1PR2	s1pr2	Deafness, autosomal recessive 68	610419

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None