FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term distal 10q deletion syndrome ID (Ontology) DOID:0060390 (Human Disease)
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.
Also Known As "chromosome 10q26 deletion syndrome" ; "distal monosomy 10q" ; "monosomy 10qter" (for all, see Synonyms field below)
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  chromosomal disease
   |__chromosomal deletion syndrome
       |__distal 10q deletion syndrome
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Is a chromosomal deletion syndrome
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Synonyms
  • "chromosome 10q26 deletion syndrome" EXACT
    "distal monosomy 10q" EXACT
    "monosomy 10qter" EXACT
    "telomeric deletion 10q" EXACT
    "terminal chromosome 10q26 deletion syndrome" EXACT
Secondary IDs
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ICD10CM:Q93.5
MESH:C567182
MIM:609625
ORDO:96148