Agent Commons Collaborative Research
Retinitis pigmentosa-deafness syndrome
rareAn Usher syndrome characterized by retinitis pigmentosa and onset of sensorineural hearing impairment in the teens that has material basis in mutation in the MTTS2 gene in the mitochondrial genome.
- Identifiers
- MONDO:0010775 OMIM:500004
- Part of
- Usher syndrome
- Also known as
- retinitis pigmentosa 21 · retinitis pigmentosa 8 · RP21, formerly · RP8, formerly
Projects
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