porphyria, acute intermittent, nonerythroid variant

Preferred Label : porphyria, acute intermittent, nonerythroid variant;

Origin ID

C566769;

UMLS CUI

C1867969;

Automatic exact mappings (from CISMeF team)
- Porphyria, acute intermittent [OMIM Phenotype]
MeSH term(s) associated for indexing
- porphyria, acute intermittent [MeSH Descriptor]
Record concept(s)
- porphyria, acute intermittent, nonerythroid variant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]