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DOID:0060398 - chromosome 16p11.2 deletion syndrome, 220kb
Disease Ontology Definition:n_a
Synonyms: distal 16p11.2 microdeletion syndrome,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
chromosomal deletion syndrome (is_a)