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Frontometaphyseal dysplasia

MONDO:0015942

Frontometaphyseal dysplasia (FMD) belongs to the otopalatodigital syndrome spectrum disorder and is characterized by anomalous ossification and skeletal patterning of the axial and appendicular skeleton, facial dysmorphism and conductive and sensorineural hearing loss.

Also known as: frontometaphyseal dysplasia, FMD

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

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Sub-types

Frontometaphyseal dysplasia 2 (2) Frontometaphyseal dysplasia 1 (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Human disease (14) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1) Disease by body system or component (0) Disease by etiologic mechanism (0)

Trials to join now! 17 Not yet recruiting 6 Not yet finished but already full! 5 Completed 8 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