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X-linked chondrodysplasia punctata

MONDO:0010556

X-linked form of chondrodysplasia punctata.

Also known as: CPXD, chondrodysplasia punctata, X-linked, X-linked dominant chondrodysplasia punctata, chondrodysplasia punctata, X-linked dominant

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

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Sub-types

X-linked chondrodysplasia punctata 1 (0) X-linked chondrodysplasia punctata 2 (0)

Broader categories

Disease (618) Metabolic disease (215) Musculoskeletal system disorder (196) Hereditary disease (172) Inherited lipid metabolism disorder (165) Bone disorder (47) Inborn errors of metabolism (42) X-linked disease (16) Human disease (14) Developmental defect during embryogenesis (7)
Trials to join now! 35 Not yet recruiting 10 Not yet finished but already full! 7 Completed 21 Terminated 1
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