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DOID:0060390 - distal 10q deletion syndrome
Disease Ontology Definition:A chromosomal deletion syndrome that is characterized by developmental delay, intellectual disability, behavioral problems and facial facies caused by a missing copy of the long arm of chromosome 10.
Synonyms: chromosome 10q26 deletion syndrome, distal monosomy 10q, monosomy 10qter, telomeric deletion 10q, terminal chromosome 10q26 deletion syndrome,
Echinobase Genes
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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)