ZFIN Human Disease: autosomal recessive nonsyndromic deafness 47

OBO ID: DOID:0110504

OBO ID: DOID:0110504

Term Name:	autosomal recessive nonsyndromic deafness 47	Search Ontology:
Synonyms:	autosomal recessive deafness 47 DFNB47
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 2p25.1-p24.3. https://www.ncbi.nlm.nih.gov/pubmed/16261342
References:	ICD10CM:H90.3 OMIM:609946
Ontology:	Human Disease ( DOID:0110504 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 47 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None