Variant Abeta2M Amyloidosis
Disease ID: disease_node_17484
Connections displayed (default: 10).
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| Dbxref | ORDO:314652 |
|---|---|
| Subclassof | DOID_0050736, DOID_655, DOID_9120 |
| Data Source | DOID |
| Synonyms | Autosomal dominant beta2-microglobulinic amyloidosis |
| Doid Label | variant ABeta2M amyloidosis |
| Doid Description | An amyloidosis that is characterized by accumulation and extensive visceral deposition of anamyloidogenic variant of beta 2 microglobulin leading to progressive gastrointestinal dysfunction, Sjögren syndrome and autonomic neuropathy. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_17484 |
| Doid Id | DOID_0080929 |
| Label | Variant Abeta2M Amyloidosis |
- Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Amyloidosis(ID:disease_node_1155) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)