hyperphenylalaninemia, Non-Pku mild

Preferred Label : hyperphenylalaninemia, Non-Pku mild;

Origin ID

C567494;

UMLS CUI

C2678416;

Automatic exact mappings (from CISMeF team)
- Phenylketonuria [OMIM Phenotype]
MeSH term(s) associated for indexing
- phenylalanine hydroxylase [MeSH Descriptor]
- phenylketonurias [MeSH Descriptor]
Record concept(s)
- hyperphenylalaninemia, Non-Pku mild [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]