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GPR143-related foveal hypoplasia

MONDO:0700230

Any foveal hypoplasia with or without albinism caused by a variant in the GPR143 gene.

Also known as: GPR143-related foveal hypoplasia with or without albinism

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

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Sub-types

Nystagmus 6, congenital, X-linked (0) X-linked recessive ocular albinism (0)

Broader categories

Disease (679) Hereditary disease (176) Human disease (14) Disease of genetic or genomic mechanism (2) Foveal hypoplasia (1) Disease by etiologic mechanism (0)

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