Inborn disorder of ornithine or proline metabolism
MONDO:0019230Also known as: disorder of ornithine or proline metabolism
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)
Autosomal recessive cutis laxa type 2
(0)
Autosomal recessive cutis laxa type 2A
(0)
Autosomal recessive cutis laxa type 2B
(0)
Autosomal recessive cutis laxa type 2C
(0)
Autosomal recessive cutis laxa type 2D
(0)
Cutis laxa, autosomal dominant 3
(0)
Hereditary spastic paraplegia 9A
(0)
Hyperprolinemia
(0)
Hyperprolinemia type 1
(0)
Hyperprolinemia type 2
(0)
Inborn disorder of ornithine metabolism
(0)
Inborn disorder of proline metabolism
(0)
P5CS deficiency
(0)
Wrinkly skin syndrome
(0)
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 amino acid and other organic acid metabolism
(0)