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, 0 tagged with Inborn disorder of biogenic amine metabolism and transport itself.
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Browse by category →Sub-types of Inborn disorder of biogenic amine metabolism and transport
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Inborn disorder of neurotransmitter metabolism and transport 0 trials · 4 incl. sub-types
4 sub-types
- Disorder of catecholamine synthesis 0 trials · 3 incl. sub-types Sub-types →
- Tyrosine hydroxylase deficiency 1 trial Sub-types →
- Brunner syndrome 0 trials
- Brain dopamine-serotonin vesicular transport disease 0 trials
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Inborn disorder of pyridoxine metabolism 0 trials · 4 incl. sub-types
2 sub-types
- Pyridoxine-dependent epilepsy 3 trials Sub-types →
- Pyridoxal phosphate-responsive seizures 2 trials
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Metabolic disease involving other neurotransmitter deficiency 0 trials · 3 incl. sub-types
3 sub-types
- Butyrylcholinesterase deficiency 3 trials
- Folinic acid-responsive seizures 0 trials
- Hereditary hyperekplexia 0 trials Sub-types →
Most studied deeper sub-types
Aromatic L-amino acid decarboxylase deficiency
(3)
Epilepsy, early-onset, vitamin B6-dependent
(1)
TH-deficient dopa-responsive dystonia
(1)
Developmental and epileptic encephalopathy, 8
(0)
Hyperekplexia 1
(0)
Hyperekplexia 2
(0)
Hyperekplexia 3
(0)
Hyperekplexia 4
(0)
Orthostatic hypotension 1
(0)
Pyridoxine-dependent epilepsy caused by ALDH7A1 mutant
(0)
TH-deficient infantile parkinsonism and motor delay
(0)
TH-deficient progressive infantile encephalopathy
(0)