Short-rib thoracic dysplasia 13 with or without polydactyly
MONDO:0014577An asphyxiating thoracic dystrophy that has material basis in homozygous mutation in the CEP120 gene on chromosome 5q23.
Also known as: SRTD13, short-rib thoracic dysplasia 13 with or without polydactyly
53 clinical trials for this condition and its sub-types.
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