chromosome 17q23.1-q23.2 deletion syndrome

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Summary

Literature (0)

DOID:0060405 - chromosome 17q23.1-q23.2 deletion syndrome

Disease Ontology Definition:A chromosomal deletion syndrome that has_material_basis_in a chromosome 17q23.1-q23.2 deletion and that is characterized by characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities.

Synonyms: 17q23.1-q23.2 microdeletion syndrome, 17q23.1q23.2 microdeletion syndrome,

Echinobase 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

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)