ZFIN Human Disease: autosomal recessive nonsyndromic deafness 5

OBO ID: DOID:0110507

OBO ID: DOID:0110507

Term Name:	autosomal recessive nonsyndromic deafness 5	Search Ontology:
Synonyms:	autosomal recessive deafness 5 DFNB5
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 14q12. https://www.ncbi.nlm.nih.gov/pubmed/8944017
References:	ICD10CM:H90.3 OMIM:600792
Ontology:	Human Disease ( DOID:0110507 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 5 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None