Apolipoprotein C-iii deficiency

Preferred Label : Apolipoprotein C-iii deficiency;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Hyperalphalipoproteinemia 2; HALP2;

Prefixed ID : #614028;

Details

Origin ID

614028;

UMLS CUI

C3151467;

Automatic exact mappings (from CISMeF team)
- APOC3 wt Allele [NCIt concept]
- apolipoprotein C-III deficiency [MeSH concept]
- apolipoprotein C-III deficiency [MeSH Supplementary Concept]
- apolipoprotein C-III deficiency [DO Concept]
DO Cross reference
- apolipoprotein C-III deficiency [DO Concept]
Genes related to phenotype
- Apolipoprotein C-iii [OMIM gene]
HPO term(s)
- Decreased LDL cholesterol concentration [HPO term]
- Hypotriglyceridemia [HPO term]
- Increased HDL cholesterol concentration [HPO term]
ORDO concept(s)
- Cholesterol-ester transfer protein deficiency [ORDO Disease]
See also inter- (CISMeF)
- Cholesterol-ester transfer protein deficiency [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- apolipoprotein C-III deficiency [MeSH Supplementary Concept]
- apolipoprotein C-III deficiency [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients