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Radioulnar synostosis, nonsyndromic, susceptibility to

MONDO:0100183

A susceptibility or predisposition to radioulnar synostosis in which the cause of the disease is a mutation in the SMAD6 gene.

5 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hereditary disease (172) Inherited disease susceptibility (69) Human disease (14) Disease susceptibility (3) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0) SMAD6-related disease (0)

Trials to join now! 4 Not yet finished but already full! 1

Quick genetic test for unborn babies hits a snag: study withdrawn

Knowledge-focused Terminated

This study aimed to see if a rapid whole genome sequencing test on amniotic fluid could give faster genetic diagnoses for fetuses with suspected genetic diseases. Researchers planned to compare results from amniotic fluid and blood samples from up to 90 families. However, the stu…

Sponsor: Mayo Clinic • Aim: Knowledge-focused

Last updated Jun 26, 2026 14:00 UTC