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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02355 | Deafness and myopia | ... the absence of other systemic, ocular, or connective tissue manifestations. DFNMYP is caused by mutations in SLITRK6. SLITRK family proteins control neurite outgrowth and regulate synaptic development. | Nervous system disease | SLITRK6 [HSA:84189] [KO:K25837] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |