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DOID:0060407 - chromosome 18q deletion syndrome
Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in a terminal deficiency or macrodeletion that is characterized by mental retardation and congenital malformations.
Synonyms: 18q- syndrome, deletion 18q, monosomy 18q,
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee