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(Q16263)
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Revision as of 20:43, 21 December 2023 by
Fire
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Created claim:
subclass of
(P1)
:
rare genetic developmental defect during embryogenesis
(Q16261)
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Statements
instance of
developmental defect during embryogenesis
0 references
rare disease
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class of disease
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subclass of
heart disease
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congenital disorder
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cardiovascular abnormality
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genetic cardiac disease
0 references
genetic disease
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rare genetic developmental defect during embryogenesis
0 references
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