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DOID:0080014 - chromosomal disease
Disease Ontology Definition:A genetic disease that has_material_basis_in extra, missing, or re-arranged chromosomes.
Synonyms:
Xenbase Genes : tbx1, sin3a, ep300, hoxd13, fgfrl1, igf2, ctbp1, fgf16, pax6, gata1, wt1, bmpr1a, gata3, hdac4, gja5,
MONDO:0019040 - chromosomal disorder |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
genetic disease (is_a)