Inborn disorder of ornithine metabolism
MONDO:0017356An inherited metabolic disease that is has its basis in the disruption of ornithine metabolic process.
Also known as: disorder of ornithine metabolism, inborn error of ornithine metabolic process, inborn ornithine metabolic process disorder, rare inborn error of ornithine metabolic process
4 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Ornithine aminotransferase deficiency
(4)
ALDH18A1-related de Barsy syndrome
(0)
Autosomal dominant complex spastic paraplegia type 9B
(0)
Autosomal dominant spastic paraplegia type 9
(0)
Autosomal recessive complex spastic paraplegia type 9B
(0)
Cutis laxa, autosomal dominant 3
(0)
Hereditary spastic paraplegia 9A
(0)
P5CS deficiency
(0)
Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Human disease
(15)
Inborn disorder of amino acid metabolism
(6)
Amino acid metabolism disease
(2)
Disease of genetic or genomic mechanism
(2)
Disease by developmental or physiological process
(0)
Disease by etiologic mechanism
(0)