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Collaborative Research
Diseases
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Syndromic disease
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Greig cephalopolysyndactyly syndrome
Greig cephalopolysyndactyly-contiguous gene syndrome
rare
Identifiers
MONDO:0958130
Orphanet:658805
Part of
Greig cephalopolysyndactyly syndrome
Multiple congenital anomalies/dysmorphic syndrome without intellectual disability
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