. . . . . . . "[X-linked dominant chondrodysplasia punctata, (CDPX2-MIM302960) also known as Conradi-H�nermann-Happle syndrome, is a rare form of skeletal dysplasia that affects the skeleton, skin, hair, and eyes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:18:01+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .