1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110404 | retinitis pigmentosa 17 | A retinitis pigmentosa characterized by relatively mild disease, with decreased visual acuity, visual field constriction, nyctalopia, and slow progression that has_material_basis_in duplication or triplication in the chromosome 17q22-q23 region that results in disruption of topologically associated domains (TADs) and increased retinal expression of GDPD1. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
