Aceruloplasminemia
Disease ID: disease_node_17441
Connections displayed (default: 10).
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| Dbxref | GARD:9499, MIM:604290 |
|---|---|
| Subclassof | DOID_655, DOID_2351, DOID_0050737 |
| Data Source | DOID |
| Doid Label | aceruloplasminemia |
| Doid Description | An iron metabolism disease that has_material_basis_in a mutation in the ceruloplasmin gene characterized by progressive neurodegeneration of the retina and basal ganglia and diabetes mellitus. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_17441 |
| Doid Id | DOID_0050711 |
| Label | Aceruloplasminemia |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Iron Metabolism Disorders(ID:disease_node_9890) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Metabolism, Inborn Errors(ID:disease_node_5171) (Disease)