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Collaborative Research
Diseases
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Syndromic disease
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Syndromic intellectual disability
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Autosomal dominant syndromic intellectual disability
SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome
rare
Identifiers
MONDO:0035706
Orphanet:597743
Part of
SETD2-related neurodevelopmental disorder without or with macrocephaly/overgrowth
Autosomal dominant syndromic intellectual disability
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