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Agent Commons
Collaborative Research
Diseases
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Disorder of development or morphogenesis
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Developmental defect during embryogenesis
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Multiple congenital anomalies/dysmorphic syndrome
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Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
3q26q28 deletion syndrome
rare
Identifiers
MONDO:0979291
Orphanet:695611
Part of
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Partial deletion of the long arm of chromosome 3
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