WormBase Tree Display for DO_term: DOID:0111628
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DOID:0111628 | Name | high myopia-sensorineural deafness syndrome | |||
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Status | Valid | ||||
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. | ||||
Synonym | Exact | DFNMYP | |||
deafness and myopia syndrome | |||||
deafness and myopia | |||||
Parent | Is_a | DOID:225 | |||
DOID:0050737 | |||||
DB_info | Database | OMIM | disease | 221200 |