Inborn disorder of phenylalanine and tyrosine metabolism
MONDO:0019235Also known as: inborn disorder of phenylalanin or tyrosine metabolism, disorder of phenylalanin or tyrosine metabolism
65 clinical trials for this condition and its sub-types, 0 tagged with Inborn disorder of phenylalanine and tyrosine metabolism itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inborn disorder of phenylalanine and tyrosine metabolism
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Disorder of phenylalanine metabolism 0 trials · 60 incl. sub-types
2 sub-types
- Phenylketonuria 57 trials · 60 incl. sub-types Sub-types →
- Tetrahydrobiopterin metabolic process disease 0 trials · 1 incl. sub-types Sub-types →
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Disorder of tyrosine metabolism 0 trials · 8 incl. sub-types
5 sub-types
- Tyrosinemia 6 trials Sub-types →
- Alkaptonuria 2 trials
- TH-deficient dopa-responsive dystonia 1 trial
- Oculocutaneous albinism type 1 0 trials · 1 incl. sub-types Sub-types →
- Hawkinsinuria 0 trials
Most studied deeper sub-types
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New PKU formula shows promise in managing blood levels
Disease control Stopped earlyThis study tested a new amino acid formula called PKU GOLIKE in people aged 16 and older with phenylketonuria (PKU). The goal was to see if it could better control daily swings in blood phenylalanine levels compared to standard treatment. The study was stopped early, so results a…
Sponsor: APR Applied Pharma Research s.a. • Aim: Disease control
Last updated Jun 27, 2026 11:00 UTC
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PKU diet in childhood may shape adult IQ, study finds
Knowledge-focused Stopped earlyThis study looks at adults with phenylketonuria (PKU) who were diagnosed as newborns and treated with a special diet. Researchers want to see if how long and how strictly they followed the diet as children affects their intelligence (IQ) as adults. The goal is to use this informa…
Sponsor: University Hospital, Lille • Aim: Knowledge-focused
Last updated Jun 27, 2026 12:37 UTC