Cure My Disease

Don't miss your cure!

Log in / Sign up

Myofibrillar myopathy 8

MONDO:0014993

Any myofibrillar myopathy in which the cause of the disease is a mutation in the PYROXD1 gene.

Also known as: PYROXD1 myofibrillar myopathy (disease), myofibrillar myopathy (disease) caused by mutation in PYROXD1, myofibrillar myopathy 8, myopathy, myofibrillar, 8, myopathy, myofibrillar, type 8, MFM8

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

Follow this condition — get notified about new trials

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Muscle tissue disorder (53) Human disease (14) Myopathy (11) Congenital myopathy (8) Skeletal muscle disorder (8) Congenital structural myopathy (5) Disease of genetic or genomic mechanism (2)

Trials to join now! 18 Not yet recruiting 7 Not yet finished but already full! 4 Completed 7 Terminated 1

Scientists gather leftover surgical tissue to unlock secrets of bone disease

Knowledge-focused Terminated

This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:52 UTC