Hyperlipidemia, familial combined, 1

Preferred Label : Hyperlipidemia, familial combined, 1;

Symbol : FCHL1;

CISMeF acronym : FCHL1; HYPLIP1;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Hyperlipidemia, combined, 1; HYPLIP1;

Prefixed ID : #602491;

Details

Origin ID

602491;

UMLS CUI

C1865289;

Currated CISMeF NLP mapping
- hyperlipidemia, combined, 1 [MeSH concept]
- hyperlipidemia, combined, 1 [MeSH Supplementary Concept]
Genes related to phenotype
- Upstream transcription factor 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- hyperlipidemia, combined, 1 [MeSH Supplementary Concept]
- hyperlipidemia, combined, 1 [MeSH concept]

Keyword's position in hierarchy(ies) :

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