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loading...| Preferred Name |
Hyperlipoproteinemia, Type I |
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| Synonyms |
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| Definitions |
A genetic disorder of lipoprotein metabolism caused by mutations in the LPL and apolipoprotein (apo) C-II genes. It is characterized by increased levels of chylomicrons and triglycerides in the blood. |
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| ID |
http://purl.obolibrary.org/obo/NCIT_C84771 |
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| code |
C84771 |
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| Contributing_Source |
Cellosaurus |
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| definition |
A genetic disorder of lipoprotein metabolism caused by mutations in the LPL and apolipoprotein (apo) C-II genes. It is characterized by increased levels of chylomicrons and triglycerides in the blood. |
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| in_subset | ||
| label |
Hyperlipoproteinemia, Type I |
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| Preferred_Name |
Hyperlipoproteinemia, Type I |
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| prefixIRI |
NCIT:C84771 |
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| prefLabel |
Hyperlipoproteinemia, Type I |
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| Semantic_Type |
Disease or Syndrome |
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| UMLS_CUI |
C0023817 |
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| subClassOf |
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