Chondrodysplasia punctata
Specialty	Medical genetics

Chondrodysplasia punctata is a clinically and genetically diverse group of rare diseases, first described by Erich Conradi (1882–1968), that share the features of stippled epiphyses and skeletal changes.^{[1]: 500 [2]: 549}

• Rhizomelic chondrodysplasia punctata 215100, 222765, 600121
• X-linked recessive chondrodysplasia punctata 302950
• Conradi–Hünermann syndrome (chondrodysplasia punctata 2, x-linked dominant) 302960
• Autosomal dominant chondrodysplasia punctata 118650

• List of cutaneous conditions
• List of radiographic findings associated with cutaneous conditions

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