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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Distal monosomy 10p
10p13-p14 deletion syndrome
rare
Identifiers
MONDO:0975905
OMIM:601362
Orphanet:687695
Part of
Distal monosomy 10p
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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