ZFIN Human Disease: autosomal recessive nonsyndromic deafness 62

OBO ID: DOID:0110514

OBO ID: DOID:0110514

Term Name:	autosomal recessive nonsyndromic deafness 62	Search Ontology:
Synonyms:	autosomal recessive deafness 62 DFNB62
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 12p13.2-p11.23. https://www.ncbi.nlm.nih.gov/pubmed/16650082
References:	ICD10CM:H90.3 OMIM:610143
Ontology:	Human Disease ( DOID:0110514 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 62 PAGES

Alliance (1)

GENES INVOLVED No data available

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None