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.
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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
Classic phenylketonuria
(4)
Maternal phenylketonuria
(3)
Mild hyperphenylalaninemia
(3)
Tyrosinemia type I
(3)
Dihydropteridine reductase deficiency
(1)
Dopa-responsive dystonia due to sepiapterin reductase deficiency
(1)
GTP cyclohydrolase I deficiency
(1)
Oculocutaneous albinism type 1A
(1)
Dystonia 5
(0)
Dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive
(0)
GTP cyclohydrolase I deficiency with hyperphenylalaninemia
(0)
Mild phenylketonuria
(0)
Minimal pigment oculocutaneous albinism type 1
(0)
Oculocutaneous albinism type 1B
(0)
Temperature-sensitive oculocutaneous albinism type 1
(0)
Tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria
(0)
Transient tyrosinemia of the newborn
(0)
Tyrosinemia type II
(0)
Tyrosinemia type III
(0)
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