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Diseases / Metabolic disease/ Amino acid metabolism disease/ Inborn disorder of amino acid metabolism/ Inborn disorder of phenylalanine and tyrosine metabolism

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 Rare Not rare Subtypes

Tetrahydrobiopterin metabolic process disease MONDO:0045014 6
Phenylalanine hydroxylase deficiency MONDO:1060259 PAH 5

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