chromosome 18p deletion syndrome

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Summary

Literature (0)

DOID:0060406 - chromosome 18p deletion syndrome

Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in partial or complete deletion of the short arm of chromosome 18.

Synonyms: 18p- syndrome, De Grouchy syndrome, monosomy 18p,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0007800 - chromosome 18p deletion syndrome

MONDO:0007800 - chromosome 18p deletion syndrome

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), chromosomal deletion syndrome (is_a)