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;

Détails

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]

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

Vous pouvez consulter :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients