8 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: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: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:2742 | auditory system disease | A sensory system disease that is characterized by auditory dysfunction located_in the auditory system. |
| DOID:2952 | inner ear disease | An auditory system disease that is located in the part of the ear that contains organs of the senses of hearing and equilibrium. |
| DOID:10003 | sensorineural hearing loss | An inner ear disease that is characterized by hearing loss resulting from damage to the cochlea, auditory nerve and/or brainstem. |
| DOID:0111751 | mitochondrial nonsyndromic sensorineural deafness | A sensorineural hearing loss that has_material_basis_in mutation in one of several different mitochondrial genes including; MTRNR1, MTTS1, MTCO1, MTTH, MTND1, and MTTI. |
7 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:10003 | DOID:0111751 |
| is_a | DOID:2742 | DOID:0111751 |
| is_a | DOID:2952 | DOID:0111751 |
| is_a | DOID:7 | DOID:0111751 |
| is_a | DOID:863 | DOID:0111751 |
| is_a | DOID:4 | DOID:0111751 |
| is_a | DOID:0050155 | DOID:0111751 |
