|OBO ID: DOID:0111628|
|Term Name:||high myopia-sensorineural deafness syndrome||Search Ontology:|
|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)|
|Ontology:||Human Disease (DOID:0111628)|
|is a type of:||
OTHER high myopia-sensorineural deafness syndrome PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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