TOR1AIP1-related multisystem disorder

MONDO:0100591

TOR1AIP1-related multisystem disorder is a rare, early-onset disorder affecting multiple organ systems that is caused by variation in the TOR1AIP1 gene. Clinical features reported in affected individuals are variable but may include hypotonia, dystonia, cerebellar atrophy, contractures, cardiomyopathy, microcephaly, cataract, deafness, skeletal anomalies, progeroid appearance and other facial dysmorphism, and nephrolithiasis.

0 clinical trials for this condition and its sub-types, 0 tagged with TOR1AIP1-related multisystem disorder itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.