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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 tyrosine metabolism

rare

Identifiers: MONDO:0017307 Orphanet:284818
Part of: Inborn disorder of phenylalanine and tyrosine metabolism

Subtypes

All diseases Rare only

Disease Rare Not rare Subtypes

Oculocutaneous albinism type 1 MONDO:0018135 4
Tyrosinemia MONDO:0004741 4
TH-deficient dopa-responsive dystonia MONDO:0011551 TH
Alkaptonuria MONDO:0008753 HGD
Hawkinsinuria MONDO:0007700 HPD

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