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Disease Chondrodysplasia punctata 2, X-linked dominant

Name Chondrodysplasia punctata 2, X-linked dominant
Synonyms CDPX2 | CDPXD | CONRADI-HUNERMANN-HAPPLE SYNDROME | CONRADI-HUNERMANN SYNDROME | CPXD | HAPPLE SYNDROME
Categories Genetic disease (inborn) | Musculoskeletal disease
MeSH® ID C538416
OMIM® ID 302960

Top ↑ Ancestors

1. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases Has associated chemicals Has associated genes Has associated exposure references Bone Diseases, Developmental Has associated chemicals Has associated genes Osteochondrodysplasias Has associated chemicals Has associated genes Chondrodysplasia Punctata Has associated chemicals Has associated genes Chondrodysplasia punctata 2, X-linked dominant Has associated chemicals Has associated genes
2. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, X-Linked Has associated chemicals Has associated genes Chondrodysplasia punctata 2, X-linked dominant Has associated chemicals Has associated genes

Top ↑ Descendants

None.