Familial Hypobetalipoproteinemia 2
Disease ID: disease_node_16841
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| Dbxref | MIM:605019 |
|---|---|
| Subclassof | DOID_1390 |
| Data Source | DOID |
| Synonyms | FHBL2, combined familial hypolipidemia |
| Doid Label | familial hypobetalipoproteinemia 2 |
| Doid Description | A hypobetalipoproteinemia that has_material_basis_in homozygous or compound heterozygous mutation in the ANGPTL3 gene on chromosome 1p31. |
| Disease Node Id | disease_node_16841 |
| Doid Id | DOID_0111061 |
| Label | Familial Hypobetalipoproteinemia 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Hypobetalipoproteinemias(ID:disease_node_4179) (Disease)