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 SLITRK6 on chromosome 13q31.1. (2)
References:
Ontology: Human Disease   (DOID:0111628)
OTHER high myopia-sensorineural deafness syndrome PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLITRK6 Deafness and myopia 221200
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None