ZFIN Human Disease: autosomal recessive nonsyndromic deafness 96

OBO ID: DOID:0110538

OBO ID: DOID:0110538

Term Name:	autosomal recessive nonsyndromic deafness 96	Search Ontology:
Synonyms:	autosomal recessive deafness 96 DFNB96
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 1p36.31-p36.13. https://www.ncbi.nlm.nih.gov/pubmed/21937999
References:	ICD10CM:H90.3 OMIM:614414
Ontology:	Human Disease ( DOID:0110538 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 96 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None