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chondrodysplasia punctata 2, X-linked dominant

Disease Summary
Associated Targets (1)
Tchem

1


Uniprot Description A clinically and genetically heterogeneous disorder characterized by punctiform calcification of the bones. The key clinical features of CDPX2 are chondrodysplasia punctata, linear ichthyosis, cataracts and short stature. CDPX2 is a rare disorder of defective cholesterol biosynthesis, biochemically characterized by an increased amount of 8-dehydrocholesterol and cholest-8(9)-en-3-beta-ol in the plasma and tissues.
Mondo Term and Equivalent IDs
MONDO:0026782:  chondrodysplasia punctata 2, X-linked dominant