Brachyolmia

MONDO:0015262

Brachyolmia is a rare, clinically and genetically heterogeneous group of bone disorders characterized by short trunk, mild short stature, scoliosis and generalized platyspondyly without significant abnormalities in the long bones.

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

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Sub-types

Autosomal dominant brachyolmia (0) Autosomal recessive brachyolmia (0) Brachyolmia, Maroteaux type (0) Brachyolmia type 1, Hobaek type (0) Brachyolmia type 1, toledo type (0)

Broader categories

Disease (717) Musculoskeletal system disorder (214) Hereditary disease (188) Bone disorder (51) Human disease (15) Osteochondrodysplasia (12) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2) Skeletal dysplasia (1)

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