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(Q1128743)
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Contiguous gene syndrome
Combined clinical phenotype caused by each missing gene in a chromosomal deletion
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Statements
subclass of
genetic disease
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Identifiers
Freebase ID
/m/04gw41p
1 reference
stated in
Freebase Data Dumps
publication date
28 October 2013
Microsoft Academic ID
2778329268
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UMLS CUI
C1855496
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Contiguous gene syndrome
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Contiguous gene syndrome
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Zespół przyległych genów
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