Chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase

Preferred Label : Chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Hyperlipoproteinemia, type ic;

Inheritance : Autosomal dominant;

Prefixed ID : %118830;

Details

Origin ID

118830;

UMLS CUI

C1861560;

Automatic exact mappings (from CISMeF team)
- Hyperlipoproteinemia type 1 [ORDO Disease]
- chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase [MeSH concept]
- chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase [MeSH Supplementary Concept]
Currated CISMeF NLP mapping
- Familial chylomicronaemia syndrome [MedDRA LLT]
- Familial chylomicronemia syndrome [ORDO Disease]
- Familial chylomicronemia syndrome [MedDRA LLT]
- familial chylomicronemia syndrome [DO Concept]
DO Cross reference
- familial chylomicronemia due to inhibition of lipoprotein lipase activity [DO Concept]
HPO term(s)
- Abdominal pain [HPO term]
- Autosomal dominant inheritance [HPO term]
- Hyperlipoproteinemia [HPO term]
- Recurrent pancreatitis [HPO term]
- Splenomegaly [HPO term]
ORDO concept(s)
- Familial chylomicronemia syndrome [ORDO Disease]
- Hyperlipoproteinemia type 1 [ORDO Disease]
See also inter- (CISMeF)
- Familial chylomicronemia syndrome (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase [MeSH Supplementary Concept]
- chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase [MeSH concept]

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