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, 0 tagged with Inborn disorder of ornithine or proline metabolism itself.
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Browse by category →Sub-types of Inborn disorder of ornithine or proline metabolism
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Inborn disorder of ornithine metabolism 0 trials · 4 incl. sub-types
2 sub-types
- Ornithine aminotransferase deficiency 4 trials
- P5CS deficiency 0 trials Sub-types →
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3 sub-types
- P5CS deficiency 0 trials Sub-types →
- Autosomal recessive cutis laxa type 2 0 trials Sub-types →
- Hyperprolinemia 0 trials Sub-types →
Most studied deeper sub-types
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 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 type 1
(0)
Hyperprolinemia type 2
(0)
Wrinkly skin syndrome
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