13 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:936 | brain disease | A central nervous system disease that is located_in the brain. |
| DOID:331 | central nervous system disease | A nervous system disease that affects either the spinal cord (myelopathy) or brain (encephalopathy) of the central nervous system. |
| 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:0050739 | autosomal genetic disease | A monogenic disease that has_material_basis_in a mutation in a single gene on one of the non-sex chromosomes. |
| DOID:0050737 | autosomal recessive disease | An autosomal genetic disease that is characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop. |
| DOID:543 | dystonia | A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements. |
| DOID:480 | movement disease | A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity. |
| DOID:0050837 | multifocal dystonia | A dystonia that involves two or more unrelated body parts. |
| DOID:0090048 | dystonia 16 | A multifocal dystonia that is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism, and that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the protein activator of interferon induced protein kinase EIF2AK2 (PRKRA) gene on chromosome 2q31. |
12 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:0050737 | DOID:0090048 |
| is_a | DOID:0050837 | DOID:0090048 |
| is_a | DOID:0050739 | DOID:0090048 |
| is_a | DOID:480 | DOID:0090048 |
| is_a | DOID:936 | DOID:0090048 |
| is_a | DOID:331 | DOID:0090048 |
| is_a | DOID:4 | DOID:0090048 |
| is_a | DOID:863 | DOID:0090048 |
| is_a | DOID:543 | DOID:0090048 |
| is_a | DOID:630 | DOID:0090048 |
| is_a | DOID:0050177 | DOID:0090048 |
| is_a | DOID:7 | DOID:0090048 |
