Short-rib thoracic dysplasia 10 with or without polydactyly
MONDO:0014284An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23.
Also known as: SRTD10, short-rib thoracic dysplasia 10 with or without polydactyly
53 clinical trials for this condition and its sub-types.
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