Orphanet: 17q21.31 microdeletion syndrome

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ORPHA:363958

Classification level: Subtype of disorder

Synonym(s):
- Del(17)(q21.31)
- Monosomy 17q21.31
Prevalence: 1-9 / 100 000
Inheritance: Autosomal dominant
Age of onset: Infancy, Neonatal
ICD-10: Q93.5
OMIM: 610443
UMLS: C1864871
MeSH: -
GARD: -
MedDRA: -

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17q21.31 microdeletion syndrome

ORPHA:363958

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