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Retinitis pigmentosa 6

MONDO:0000910

A retinitis pigmentosa that has material basis in variation in the chromosome region Xp21.3-p21.2.

Also known as: RP6, retinitis pigmentosa 6, retinitis pigmentosa type 6, RP 6, retinitis pigmentosa, X-linked recessive, 6

33 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Eye disorder (97) Retinal disorder (79) Retinitis pigmentosa (74) Inherited retinal dystrophy (40) Retinal degeneration (40) Perceptual disorders (21) X-linked disease (16)
Trials to join now! 21 Not yet recruiting 3 Not yet finished but already full! 1 Completed 6 Terminated 2
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