Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Ornithine aminotransferase deficiency

MONDO:0009796

A very rare inherited retinal dystrophy characterized by progressive chorioretinal atrophy, myopia and early cataract.

Also known as: GACR, HOGA, gyrate atrophy, gyrate atrophy of choroid and retina with or without ornithinemia, hoga, hyperornithinemia, hyperornithinemia-gyrate atrophy of choroid and retina syndrome, ornithine aminotransferase deficiency

35 clinical trials for this condition and its sub-types, 4 tagged with Ornithine aminotransferase deficiency itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by