ZFIN Human Disease: autosomal recessive nonsyndromic deafness 25

OBO ID: DOID:0110483

Term Name:	autosomal recessive nonsyndromic deafness 25		Search Ontology:
Synonyms:	autosomal recessive deafness 25 DFNB25
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with moderate to profound, progressive hearing loss and has_material_basis_in mutation in the GRXCR1 gene on chromosome 4p13. https://www.ncbi.nlm.nih.gov/pubmed/20137778
References:	ICD10CM:H90.3 OMIM:613285
Ontology:	Human Disease ( DOID:0110483 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 25 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
GRXCR1	grxcr1a grxcr1b	Deafness, autosomal recessive 25	613285

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None