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Up to: Autosomal recessive disease · Acromelic dysplasia · Jeune syndrome · IFT140-related recessive ciliopathy
Short-rib thoracic dysplasia 9 with or without polydactyly
An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT140 gene on chromosome 16p13.
This condition has no sub-types.