Cure My Disease

Don't miss your cure!

Log in / Sign up

Craniometaphyseal dysplasia

MONDO:0015465

Craniometaphyseal dysplasia (CMD) is a very rare genetic bone disease characterized by progressive diffuse hyperostosis of cranial bones causing facial dysmorphism and functional repercussions, and metaphyseal widening of long bones.

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

Follow this condition — get notified about new trials

Sub-types

Craniometaphyseal dysplasia, autosomal dominant (1) Craniodiaphyseal dysplasia (0) Craniodiaphyseal dysplasia, autosomal dominant (0) Craniometaphyseal dysplasia, autosomal recessive (0)

Broader categories

Disease (618) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Human disease (14) Bone remodeling disease (5) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Osteosclerosis (1) Disease by body system or component (0)

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