ZFIN Human Disease: autosomal recessive nonsyndromic deafness 86

OBO ID: DOID:0110532

Term Name:	autosomal recessive nonsyndromic deafness 86		Search Ontology:
Synonyms:	autosomal recessive deafness 86 DFNB86
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TBC1D24 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/24387994
References:	ICD10CM:H90.3 OMIM:614617
Ontology:	Human Disease ( DOID:0110532 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 86 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TBC1D24	tbc1d24	Deafness, autosomal recessive 86	614617

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None