ZFIN Human Disease: autosomal recessive nonsyndromic deafness 32

OBO ID: DOID:0110491

Term Name:	autosomal recessive nonsyndromic deafness 32		Search Ontology:
Synonyms:	autosomal recessive deafness 32 DFNB32 hearing impairment infertile male syndrome HIIMS
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and male infertility in some affected men that has_material_basis_in mutation in the CDC14A gene on chromosome 1p21.2. (2)
References:	ICD10CM:H90.3 OMIM:608653
Ontology:	Human Disease ( DOID:0110491 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 32 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CDC14A	cdc14aa cdc14ab	Deafness, autosomal recessive 32, with or without immotile sperm	608653

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None