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distal 10q deletion syndrome (DOID:0060390)
Alliance: disease page
Synonyms: chromosome 10q26 deletion syndrome; distal monosomy 10q; monosomy 10qter; telomeric deletion 10q; terminal chromosome 10q26 deletion syndrome
Alt IDs: OMIM:609625, ICD10CM:Q93.5, MESH:C567182, ORDO:96148
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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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11/12/2024
MGI 6.24 		The Jackson Laboratory