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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

MONDO:0012830 - chromosome 10q23 deletion syndrome |
MIM:612242 - CHROMOSOME 10q22.3-q23.2 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)