ZFIN Human Disease: autosomal recessive nonsyndromic deafness 13

OBO ID: DOID:0110468

OBO ID: DOID:0110468

Term Name:	autosomal recessive nonsyndromic deafness 13	Search Ontology:
Synonyms:	autosomal recessive deafness 13 DFNB13
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 7q34-q36. https://www.ncbi.nlm.nih.gov/pubmed/9781028
References:	ICD10CM:H90.3 OMIM:603098
Ontology:	Human Disease ( DOID:0110468 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 13 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None