Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

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.

2 clinical trials for this condition and its sub-types, 1 tagged with Craniometaphyseal dysplasia itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Familial osteosclerosis (16)

Sub-types of Craniometaphyseal dysplasia

Craniometaphyseal dysplasia, autosomal dominant 1 trial
Craniodiaphyseal dysplasia 0 trials
Craniodiaphyseal dysplasia, autosomal dominant 0 trials
Craniometaphyseal dysplasia, autosomal recessive 0 trials

Including sub-types (2) Tagged with Craniometaphyseal dysplasia (1)

Trials to join now! 1 Not yet recruiting 1

Hunt for genes behind rare bone disease could unlock future treatments

Knowledge-focused Recruiting now

This study aims to find the genes and genetic changes that cause craniometaphyseal dysplasia (CMD), a rare disorder that leads to abnormal bone growth in the skull and other bones. Researchers will analyze blood and tissue samples from 600 people, including affected individuals a…

Sponsor: UConn Health • Aim: Knowledge-focused

Last updated Jun 27, 2026 12:09 UTC