Inborn disorder of biogenic amine metabolism and transport
MONDO:0019250Also known as: disorder of biogenic amine metabolism and transport
10 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Aromatic L-amino acid decarboxylase deficiency
(3)
Butyrylcholinesterase deficiency
(3)
Pyridoxine-dependent epilepsy
(3)
Pyridoxal phosphate-responsive seizures
(2)
Epilepsy, early-onset, vitamin B6-dependent
(1)
TH-deficient dopa-responsive dystonia
(1)
Tyrosine hydroxylase deficiency
(1)
Brain dopamine-serotonin vesicular transport disease
(0)
Brunner syndrome
(0)
Developmental and epileptic encephalopathy, 8
(0)
Disorder of catecholamine synthesis
(0)
Folinic acid-responsive seizures
(0)
Hereditary hyperekplexia
(0)
Hyperekplexia 1
(0)
Hyperekplexia 2
(0)
Hyperekplexia 3
(0)
Hyperekplexia 4
(0)
Inborn disorder of neurotransmitter metabolism and transport
(0)
Inborn disorder of pyridoxine metabolism
(0)
Metabolic disease involving other neurotransmitter deficiency
(0)