11 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:10124 | corneal disease | An eye disease that affects the cornea, which is the transparent surface of the eye that assists in light refraction. |
| 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. |
| DOID:5614 | eye disease | An eye and adnexa disease that is located_in the eye. |
| 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). |
| DOID:0050177 | monogenic disease | A genetic disease that is the result of one or more abnormal alleles and may be dominant, semi-dominant, or recessive. |
| DOID:630 | genetic disease | A disease that has_material_basis_in genetic variations in the human genome. |
| DOID:2566 | corneal dystrophy | |
| DOID:0060457 | posterior polymorphous corneal dystrophy | A corneal dystrophy that is characterized by changes in Descemet's membrane and endothelial layer. |
| DOID:0110857 | posterior polymorphous corneal dystrophy 3 | A posterior polymorphous corneal dystrophy that has_material_basis_in heterozygous mutation in the ZEB1 gene on chromosome 10p11.22. |
10 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050177 | DOID:0110857 |
| is_a | DOID:0060457 | DOID:0110857 |
| is_a | DOID:863 | DOID:0110857 |
| is_a | DOID:630 | DOID:0110857 |
| is_a | DOID:4 | DOID:0110857 |
| is_a | DOID:0050155 | DOID:0110857 |
| is_a | DOID:10124 | DOID:0110857 |
| is_a | DOID:2566 | DOID:0110857 |
| is_a | DOID:5614 | DOID:0110857 |
| is_a | DOID:7 | DOID:0110857 |
