Prion Diseases
Disease ID: disease_node_9041
Connections displayed (default: 10).
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| Dbxref | ICD10CM:A81.9, KEGG:05020, MESH:D017096, NCI:C128346, SNOMEDCT_US_2023_03_01:20484008, UMLS_CUI:C0162534 |
|---|---|
| Subclassof | DOID_936, DOID_0050117 |
| Data Source | DOID, MESH |
| Synonyms | Prion disease pathway, Prion protein disease, Spongiform Encephalopathy, prion induced disorder, transmissible spongiform encephalopathy |
| Mesh Id | D017096 |
| Mesh Label | Prion Diseases |
| Mesh Subclassof | D019636, D002494 |
| Doid Label | prion disease |
| Doid Description | A brain disease that is characterized by brain damage resulting from the abnormal folding, clumping and accumulation of cellular proteins in the brain induced by prion proteins. |
| Disease Node Id | disease_node_9041 |
| Doid Id | DOID_649 |
| Label | Prion Diseases |
- Incoming r'ship
SUBCLASS_OFto/from Wasting Disease, Chronic(ID:disease_node_11100) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Scrapie(ID:disease_node_6808) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Brain Diseases(ID:disease_node_1682) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Disease By Infectious Agent(ID:disease_node_15361) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Kuru(ID:disease_node_4538) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Insomnia, Fatal Familial(ID:disease_node_11096) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Huntington'S Disease-Like 1(ID:disease_node_15362) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Gerstmann-Straussler-Scheinker Disease(ID:disease_node_8552) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Creutzfeldt-Jakob Syndrome(ID:disease_node_4358) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Encephalopathy, Bovine Spongiform(ID:disease_node_8830) (Disease)