Short-rib thoracic dysplasia 7 with or without polydactyly

MONDO:0013569

An asphyxiating thoracic dystrophy that has material basis in homozygous or compound heterozygous mutation in the WDR35 gene on chromosome 2p21.1.

Also known as: SRPS5, SRTD7, short rib-polydactyly syndrome type 5, short rib-polydactyly syndrome, type 5, short-rib thoracic dysplasia 7 with or without polydactyly

1 clinical trial for this condition and its sub-types, 0 tagged with Short-rib thoracic dysplasia 7 with or without polydactyly itself.

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Part of

↑ Jeune syndrome (2)

Including sub-types (1) Tagged with Short-rib thoracic dysplasia 7 with or without polydactyly (0)

Trials to join now! 1

Could a diabetes drug protect kidneys in children with genetic disease?

Disease control Recruiting now

This study tests whether adding dapagliflozin (a diabetes drug) to standard care reduces protein leakage in the urine of children with hereditary kidney diseases. About 44 children will receive either dapagliflozin plus standard care or standard care alone for 12 weeks, then swit…

Phase 3 • Sponsor: Children's Hospital of Fudan University • Aim: Disease control

Last updated Jul 08, 2026 00:00 UTC

Short-rib thoracic dysplasia 7 with or without polydactyly

Where it sits in the disease tree

Could a diabetes drug protect kidneys in children with genetic disease?