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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 due to 14q32.2 imprinting defect
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Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
Maternal 14q32.2 hypermethylation syndrome
rare
Identifiers
MONDO:0016783
Orphanet:254534
Part of
Multiple congenital anomalies due to 14q32.2 maternally expressed gene defect
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