Leigh Disease
Disease ID: disease_node_4615
Connections displayed (default: 10).
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| Dbxref | GARD:6877, ICD10CM:G31.82, MESH:D007888, MIM:256000, NCI:C84814, ORDO:506, SNOMEDCT_US_2023_03_01:29570005, UMLS_CUI:C0023264 |
|---|---|
| Subclassof | DOID_3762 |
| Data Source | DOID, MESH |
| Synonyms | Infantile necrotizing encephalomyelopathy, Leigh syndrome, juvenile subacute necrotizing encephalomyelopathy, subacute necrotizing encephalomyelopathy |
| Mesh Id | D007888 |
| Mesh Label | Leigh Disease |
| Mesh Subclassof | D028361, D015323, D020739 |
| Doid Label | Leigh disease |
| Doid Description | A cytochrome-c oxidase deficiency disease characterized by progressive loss of mental and movement abilities. Symptoms usually begin between ages of three months and two years and include loss of appetite, vomiting, irritability and seizure activity. Xref MGI. OMIM mapping confirmed by DO. [SN]. |
| Has Symptom | SYMP_0000124, SYMP_0000654, SYMP_0000309, SYMP_0019145 |
| Disease Node Id | disease_node_4615 |
| Doid Id | DOID_3652 |
| Label | Leigh Disease |
- Outgoing r'ship
HAS_SYMPTOMto/from Vomiting(ID:disease_node_7914;disease_node_20962) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Loss Of Appetite(ID:disease_node_21484) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Seizure(ID:disease_node_21382) (Disease) - Outgoing r'ship
HAS_SYMPTOMto/from Irritability(ID:disease_node_21405) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Cytochrome-C Oxidase Deficiency(ID:disease_node_11065) (Disease)