Neurodegenerative Diseases
Disease ID: disease_node_9989
Connections displayed (default: 10).
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| Dbxref | ICD10CM:G31.9, MESH:D019636, NCI:C27090, SNOMEDCT_US_2023_03_01:362975008, UMLS_CUI:C0524851, UMLS_CUI:C1285162 |
|---|---|
| Subclassof | DOID_331 |
| Data Source | DOID, MESH |
| Synonyms | degenerative disease |
| Mesh Id | D019636 |
| Mesh Label | Neurodegenerative Diseases |
| Mesh Subclassof | D009422 |
| Doid Label | neurodegenerative disease |
| Doid Description | A central nervous system disease that results in the progressive deterioration of function or structure of neurons. |
| Disease Node Id | disease_node_9989 |
| Doid Id | DOID_1289 |
| Label | Neurodegenerative Diseases |
| Doid Alternate Ids | DOID_4874 |
- Incoming r'ship
SUBCLASS_OFto/from Tauopathies(ID:disease_node_10941) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Stress-Induced Childhood-Onset Neurodegeneration With Variable Ataxia And Seizures(ID:disease_node_16102) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Synucleinopathy(ID:disease_node_16122) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Spinocerebellar Degenerations(ID:disease_node_7048) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Parkinson Disease, Secondary(ID:disease_node_5926) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Plexopathy(ID:disease_node_16090) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Neuronal Intranuclear Inclusion Disease(ID:disease_node_16099) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Olivopontocerebellar Atrophies(ID:disease_node_5684) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Neurodevelopmental Disorder With Regression, Abnormal Movements, Loss Of Speech, And Seizures(ID:disease_node_16097) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Central Nervous System Diseases(ID:disease_node_1915) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Neurodegeneration With Ataxia, Dystonia, And Gaze Palsy, Childhood-Onset(ID:disease_node_16100) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Myoclonic Cerebellar Dyssynergia(ID:disease_node_1922) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Huntington'S Disease-Like 2(ID:disease_node_16098) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Hereditary Ataxia(ID:disease_node_16048) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Infantile Cerebellar-Retinal Degeneration(ID:disease_node_16142) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Huntington Disease(ID:disease_node_4042) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Childhood-Onset Neurodegeneration With Brain Atrophy(ID:disease_node_16101) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Amyotrophic Lateral Sclerosis(ID:disease_node_1156) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Agenesis Of The Corpus Callosum With Peripheral Neuropathy(ID:disease_node_16096) (Disease)
- Incoming r'ship
ASSOCIATED_WITH_DISEASEto/from Passiflora foetida (Plant) Rel Props:Doid:DOID_1289; Mesh:D019636; Part:fruit; leaf; Reference:ISBN:9789327275590 - Incoming r'ship
ASSOCIATED_WITH_DISEASEto/from Gardenia gummifera (Plant) Rel Props:Doid:DOID_1289; Mesh:D019636; Part:fruit; Reference:ISBN:9789327275590 - Incoming r'ship
ASSOCIATED_WITH_DISEASEto/from Ferula assa-foetida (Plant) Rel Props:Doid:DOID_1289; Mesh:D019636; Part:whole plant; Reference:ISBN:9789327275590