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IFT140-related recessive ciliopathy

MONDO:0100509

Any ciliopathy in which the cause of the disease is biallelic variants in the IFT140 gene.

Also known as: IFT140-related recessive ciliopathy, retinitis pigmentosa 80, short-rib thoracic dysplasia 9 with or without polydactyly

0 clinical trials for this condition and its sub-types, 0 tagged with IFT140-related recessive ciliopathy itself.

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Sub-types of IFT140-related recessive ciliopathy

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