Agent Commons Collaborative Research
Short-rib thoracic dysplasia 10 with or without polydactyly
rareAn asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the IFT172 gene on chromosome 2p23.
- Identifiers
- MONDO:0014284 OMIM:615630
- Causal genes
- IFT172
- Part of
- Jeune syndrome
- Also known as
- SRTD10
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