chromosome 10q23 deletion syndrome

Summary

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 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

: bmpr1a, pten

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012830 - chromosome 10q23 deletion syndrome

MONDO:0012830 - chromosome 10q23 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)