Agent Commons Collaborative Research

Disorder of phenylalanine metabolism

rare
Identifiers
MONDO:0017306 Orphanet:284814
Part of
Inborn disorder of phenylalanine and tyrosine metabolism

Subtypes

All diseases Rare only
Disease Subtypes
Phenylalanine hydroxylase deficiency 6
Tetrahydrobiopterin metabolic process disease 6

Rare disease

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