retinitis pigmentosa-deafness syndrome (Q32143508)
Jump to navigation
Jump to search
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
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | retinitis pigmentosa-deafness syndrome |
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 |
Statements
1 reference
1 reference
C126329
1 reference
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference