hypobetalipoproteinemia, familial, 2

Preferred Label : hypobetalipoproteinemia, familial, 2;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566032;

UMLS CUI

C1857970;

Currated CISMeF NLP mapping
- Familial hypobetalipoproteinemia [ORDO Disease]
- Familial hypobetalipoproteinemia (disorder) [SNOMED CT concept]
- Hypobetalipoproteinemia, familial, 2 [OMIM Phenotype]
- familial hypobetalipoproteinemia [SNOMED Notion]
- familial hypobetalipoproteinemia 2 [DO Concept]
Related record
- hypobetalipoproteinemia, familial, 2 [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hypobetalipoproteinemia, familial, 2 [OMIM Phenotype]
- familial hypobetalipoproteinemia 2 [DO Concept]