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DOID:0060413 - chromosome 22q11.2 deletion syndrome, distal
Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome 22q11.2 region, distinct from DiGeorge syndrome and velocardiofacial syndrome.
Synonyms: 22q11.2 deletion syndrome, DiGeorge syndrome and Velocardiofacial syndrome, distal 22q11.2 microdeletion syndrome
Xenbase Genes

MONDO:0012740 - chromosome 22q11.2 deletion syndrome, distal |
MIM:611867 - CHROMOSOME 22q11.2 DELETION SYNDROME, DISTAL |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal deletion syndrome (is_a)