|
DOID:0060293 - autosomal dominant chondrodysplasia punctata
Disease Ontology Definition:n_a
Synonyms:
Xenbase Genes :
MONDO:0007321 - autosomal dominant chondrodysplasia punctata |
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)