1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0110120 | Axenfeld-Rieger syndrome type 1 | An Axenfeld-Rieger syndrome that has_material_basis_in heterozygous mutation in the homeobox transcription factor gene PITX2 on chromosome 4q25. |
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). |
