Hyperchylomicronemia
Symptom Information:
Symptom ID: | HPO:0012238 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of lipid metabolism(HPO:0003119) Abnormality of cholesterol metabolism(HPO:0003107) Abnormality of the level of lipoprotein cholesterol(HPO:0010979) Hyperlipoproteinemia(HPO:0010980) Hyperchylomicronemia(HPO:0012238) MedDRA: Investigations(MedDRA:10022891) Lipid analyses(MedDRA:10024580) Cholesterol analyses(MedDRA:10008651) Hyperchylomicronemia(HPO:0012238) |
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Database Frequency: | 2 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Hyperlipoproteinemia type 5 | (Orphanet:70470) |