ZFIN Human Disease: autosomal recessive nonsyndromic deafness 98

OBO ID: DOID:0110540

Term Name:	autosomal recessive nonsyndromic deafness 98		Search Ontology:
Synonyms:	autosomal recessive deafness 98 DFNB98
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TSPEAR gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/22678063
References:	ICD10CM:H90.3 OMIM:614861
Ontology:	Human Disease ( DOID:0110540 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 98 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TSPEAR	tspearb tspeara	?Deafness, autosomal recessive 98	614861

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None