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Disease Ontology Browser
high myopia-sensorineural deafness syndrome (DOID:0111628)
Alliance: disease page
Synonyms: deafness and myopia; deafness and myopia syndrome; DFNMYP
Alt IDs: OMIM:221200, ORDO:363396
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.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
05/26/2020
MGI 6.15
The Jackson Laboratory