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Temple syndrome due to paternal 14q32.2 microdeletion

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ORPHA:254525

Classification level: Subtype of disorder

Synonym(s):
  • Paternal del(14)(q32.2)

Prevalence: <1 / 1 000 000

Inheritance: Autosomal dominant, Not applicable

Age of onset: Infancy, Neonatal

ICD-10: Q93.5

ICD-11: LD44.E

OMIM: 616222

UMLS: C5679639

Summary

This disease is described under Temple syndrome

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