1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111021 | cone-rod dystrophy 15 | A cone-rod dystrophy that has_material_basis_in homozygous mutation in the CDHR1 gene on chromosome 10q23. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0050155 | sensory system disease | A nervous system disease which is located in a part of the nervous system responsible for processing sensory information that consists of sensory receptors, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, somatic sensation (touch), taste and olfaction (smell). |
