ZFIN Human Disease: autosomal recessive nonsyndromic deafness 71

OBO ID: DOID:0110522

OBO ID: DOID:0110522

Term Name:	autosomal recessive nonsyndromic deafness 71	Search Ontology:
Synonyms:	autosomal recessive deafness 71 DFNB71
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 8p22-p21.3. https://www.ncbi.nlm.nih.gov/pubmed/19229252
References:	ICD10CM:H90.3 OMIM:612789
Ontology:	Human Disease ( DOID:0110522 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 71 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None