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Summary Literature (0)
DOID:0060389 - chromosome 10q23 deletion syndrome


Disease Ontology Definition:A chromosomal deletion syndrome that is characterized by dysmorphic facies, developmental delay and multiple congenital abnormalities and huvenile polyposis, has_material_basis_in recurrent deletions of chromosome 10q22.3-q23.2.

Synonyms:

Xenbase Genes : bmpr1a, pten

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012830 - chromosome 10q23 deletion syndrome

OMIM:
OMIM:612242 - CHROMOSOME 10q22.3-q23.2 DELETION SYNDROME

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)