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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 the SLITRK6 gene on chromosome 13q31.1.

Disease References using Mouse Models (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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12/10/2024
MGI 6.24 		The Jackson Laboratory