Hyperchylomicronemia

Preferred Label : Hyperchylomicronemia;

Inclusion CIM-10 : Hyperlipidemia, group D; Mixed hyperglyceridemia; Fredrickson's hyperlipoproteinemia, type I or V; Chylomicron retention disease;

Diag associé à un acte (%) : 60.8;

Source : OMS;

Date de début : 01/01/1997;

Détails

Origin ID

E783;

UMLS CUI

C0023817;

Automatic exact mappings (from CISMeF team)
- Chylomicron retention disease [ORDO Disease]
- Chylomicron retention disease [ICD-11 More detail]
- Chylomicron retention disease [OMIM Phenotype]
- Chylomicron retention disease (disorder) [SNOMED CT concept]
- Hyperchylomicronemia [MedDRA LLT]
- Hyperchylomicronemia [PASCAL descriptor]
- Increased circulating chylomicron concentration [HPO term]
- chylomicron retention disease [DO Concept]
CISMeF manual mappings
- Familial lipoprotein lipase deficiency with type I phenotype (disorder) [SNOMED CT concept]
- Fredrickson type I hyperlipoproteinemia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Familial hyperchylomicronemia (disorder) [SNOMED CT concept]
- Hyperchylomicronaemia [MedDRA Preferred Term]
- Hyperchylomicronemia [ICD-9 code]
- familial lipoprotein lipase deficiency [DO Concept]
DO Cross reference
- chylomicron retention disease [DO Concept]
- familial lipoprotein lipase deficiency [DO Concept]
Orphanet concepts
- Familial GPIHBP1 deficiency [ORDO Disease]
- Familial apolipoprotein A5 deficiency [ORDO Disease]
- Familial apolipoprotein C-II deficiency [ORDO Disease]
- Familial chylomicronemia syndrome [ORDO Disease]
- Familial lipase maturation factor 1 deficiency [ORDO Disease]
- Familial lipoprotein lipase deficiency [ORDO Disease]
- Hyperlipoproteinemia type 1 [ORDO Disease]
- Hyperlipoproteinemia type 5 [ORDO Disease]
- Rare dyslipidemia [ORDO Disease]
- Rare hyperlipidemia [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Familial hyperchylomicronemia (disorder) [SNOMED CT concept]
- Familial lipoprotein lipase deficiency [ORDO Disease]
- Familial lipoprotein lipase deficiency [ICD-11 More detail]
- Familial lipoprotein lipase deficiency (disorder) [SNOMED CT concept]
- Familial lipoprotein lipase deficiency with type I phenotype (disorder) [SNOMED CT concept]
- Fredrickson type I hyperlipoproteinemia (disorder) [SNOMED CT concept]
- Hyperchylomicronemia [MedDRA LLT]
- Hyperchylomicronemia [ICD-9 code]
- Hyperlipoproteinemia type 1 [ORDO Disease]
- Hyperlipoproteinemia, Type I [NCIt concept]
- Hyperlipoproteinemia, type I [OMIM Phenotype]
- Lipoprotein-lipase deficiency [MedDRA LLT]
- Type I hyperlipoproteinaemia [MedDRA LLT]
- Type I hyperlipoproteinemia [MedDRA LLT]
- familial lipoprotein lipase deficiency [SNOMED Notion]
- familial lipoprotein lipase deficiency [DO Concept]
- hyperlipoproteinemia type I [MeSH concept]
- hyperlipoproteinemia type i [MeSH Descriptor]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients