|
DOID:0060388 - chromosomal deletion syndrome
Disease Ontology Definition:A chromosomal disease that has_material_basis_in partial deletion of chromosomes.
Synonyms:
Xenbase Genes : tbx1, sin3a, ep300, fgfrl1, ctbp1, pax6, wt1, bmpr1a, gata3, hdac4, gja5, pten, gja8, mlxipl, irf1,
MONDO:0000761 - syndrome caused by partial chromosomal deletion |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal disease (is_a)