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Summary Literature (0)
DOID:0060427 - chromosome Xp21 deletion syndrome

Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region.

Synonyms: Xp21 microdeletion syndrome, complex glycerol kinase deficiency, monosomy Xp21,

Xenbase Genes :

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010399 - chromosome Xp21 deletion syndrome


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)