Hypertriglyceridemia 2 - CISMeF

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CISMeF

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Hypertriglyceridemia 2OMIM Phenotype

Preferred Label : Hypertriglyceridemia 2;

Symbol : HYTG2;

Type : Phenotype, molecular basis known;

Prefixed ID : #619324;

Details

Origin ID

619324;

UMLS CUI

C5543398;

Genes related to phenotype
- Camp response element-binding protein 3-like 3 [OMIM gene]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Decreased HDL cholesterol concentration [HPO term]
- Hypercholesterolemia [HPO term]
- Hypertriglyceridemia [HPO term]
ORDO concept(s)
- Transient infantile hypertriglyceridemia and hepatosteatosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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09/05/2025

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