Concept information
...
disease, disability, health, and health behavior
disease
metabolic disorders
inborn errors of metabolism
...
disease, disability, health, and health behavior
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
...
the social context of careers - ethnicity, gender, and diversity
disability
congenital disorders
inborn errors of metabolism
Terme préférentiel
phenylketonuria
Définition
- Phenylketonuria (PKU) is an inherited genetic disorder that increases blood levels of the essential amino acid phenylalanine (a building block of protein). It is normally obtained through the diet in regulated levels. [Source: Encyclopedia of Global Health; Phenylketonuria]
Concept générique
Appartient au groupe
URI
http://data.loterre.fr/ark:/67375/N9J-QGFGVQ9R-S
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