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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.

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Sub-types

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

Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) 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! 1 Not yet recruiting 1
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