ZFIN Human Disease: high myopia-sensorineural deafness syndrome

OBO ID: DOID:0111628

Term Name:	high myopia-sensorineural deafness syndrome		Search Ontology:
Synonyms:	deafness and myopia deafness and myopia syndrome DFNMYP
Definition:	A syndrome characterized by severe myopia and moderate to profound, bilateral, progressive sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the SLITRK6 gene on chromosome 13q31.1. (2)
References:	GARD:12844 OMIM:221200 ORDO:363396
Ontology:	Human Disease ( DOID:0111628 )

Relationships

is a type of:	autosomal recessive disease syndrome autosomal recessive disease syndrome Show first 5 Terms

OTHER high myopia-sensorineural deafness syndrome PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SLITRK6	slitrk6	Deafness and myopia	221200

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None