FLVCR1-related retinopathy with or without ataxia

MONDO:0100449

A disorder characterized by retinopathy with ataxia in most patients, caused by biallelic variants in the FLVCR1 gene.

Also known as: FLVCR1 retinopathy with or without ataxia, AXPC1, PCARP, ataxia, posterior column, with retinitis pigmentosa, autosomal recessive posterior column ataxia and retinitis pigmentosa, posterior column ataxia with retinitis pigmentosa, posterior column ataxia-retinitis pigmentosa syndrome

44 clinical trials for this condition and its sub-types, 0 tagged with FLVCR1-related retinopathy with or without ataxia itself.

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Part of

↑ Inherited retinal dystrophy (513) ↑ Autosomal recessive degenerative and progressive cerebellar ataxia (49)

Sub-types of FLVCR1-related retinopathy with or without ataxia

Posterior column ataxia-retinitis pigmentosa syndrome 1 trial

Including sub-types (44) Tagged with FLVCR1-related retinopathy with or without ataxia (0)

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