RS140967266 IFT172
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Associated Conditions
Short-rib thoracic dysplasia 10 with or without polydactyly
Retinitis pigmentosa 71
Inborn genetic diseases
Short-rib thoracic dysplasia 10 with or without polydactyly
Retinitis pigmentosa 71
Inborn genetic diseases
Other Variants in IFT172