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15q24 microdeletion syndrome

Disease definition

15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.

ORPHA:94065

Classification level: Subtype of disorder
  • Synonym(s):
    • Del(15)(q24)
    • Monosomy 15q24
  • Prevalence: <1 / 1 000 000
  • Inheritance: Not applicable or Unknown 
  • Age of onset: Childhood
  • ICD-10: Q93.5
  • OMIM: 613406
  • UMLS: C3697269
  • MeSH: -
  • GARD: -
  • MedDRA: -

Detailed information

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