Amyotrophic Lateral Sclerosis
Disease ID: disease_node_1156
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| Dbxref | GARD:9239, MESH:D000690, MIM:105500, ORDO:90020, SNOMEDCT_US_2023_03_01:62239001, UMLS_CUI:C0543859 |
|---|---|
| Subclassof | DOID_1289 |
| Data Source | DOID, MESH |
| Synonyms | ALS-PDC, Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome, Guam disease, Lytico-Bodig disease, PDALS, amyotrophic lateral sclerosis-parkinsonism/dementia complex of Guam, parkinsonism-dementia-ALS complex |
| Mesh Id | D000690 |
| Mesh Label | Amyotrophic Lateral Sclerosis |
| Mesh Subclassof | D016472, D057177, D013118 |
| Doid Label | amyotrophic lateral sclerosis-parkinsonism/dementia complex 1 |
| Doid Description | A neurodegenerative disease characterized by chronic, progressive amyotrophic lateral sclerosis and parkinsonism-dementia. Susceptibility to this disease is influenced by heterozygous mutation in TRPM7 on 15q21.2. |
| Disease Node Id | disease_node_1156 |
| Doid Id | DOID_0111246 |
| Label | Amyotrophic Lateral Sclerosis |
- Outgoing r'ship
SUBCLASS_OFto/from Neurodegenerative Diseases(ID:disease_node_9989) (Disease)