Inborn disorder of pyridoxine metabolism
MONDO:0019237An inherited metabolic disease that is has its basis in the disruption of pyridoxine metabolic process.
Also known as: inborn error of pyridoxine metabolic process, inborn pyridoxine metabolic process disorder, rare inborn error of pyridoxine metabolic process, disorder of pyridoxine metabolism
4 clinical trials for this condition and its sub-types.
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Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)
Inborn disorder of biogenic amine metabolism and transport
(0)