Familial Chylomicronemia Syndrome
Disease ID: disease_node_16845
Connections displayed (default: 10).
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| Dbxref | ORDO:444490 |
|---|---|
| Subclassof | DOID_1168 |
| Data Source | DOID |
| Doid Label | familial chylomicronemia syndrome |
| Doid Description | A familial hyperlipidemia characterized by hypertriglyceridemia and fasting chylomicronemia. |
| Disease Node Id | disease_node_16845 |
| Doid Id | DOID_0111417 |
| Label | Familial Chylomicronemia Syndrome |
- Incoming r'ship
SUBCLASS_OFto/from Hyperlipoproteinemia Type I(ID:disease_node_4796) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyperlipidemias(ID:disease_node_4103) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Hyperlipoproteinemias(ID:disease_node_4108) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Apolipoprotein A5 Deficiency(ID:disease_node_16847) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Gpihbp1 Deficiency(ID:disease_node_16848) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Chylomicronemia Due To Inhibition Of Lipoprotein Lipase Activity(ID:disease_node_16849) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Familial Lipase Maturation Factor 1 Deficiency(ID:disease_node_16846) (Disease)