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DOID:0060292 - X-linked chondrodysplasia punctata
Disease Ontology Definition:n_a
Synonyms: chondrodystrophia calcificans congenita,
Echinobase Genes : ebp
MIM:302950 - chondrodysplasia punctata 1, x-linked recessive; cdpx1 |
MIM:302960 - chondrodysplasia punctata 2, x-linked dominant; cdpx2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chondrodysplasia punctata (is_a)