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Abnormality, Cardiovascular (MeSH) - C0243050 L0276718 S0793306 A0852592 M0027602 MeSH PM D018376 → |
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Abnormality, Chromosomal - C0008625 L0276719 S0325478 A0359451 M0004406 MeSH PM D002869 → |
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Abnormality, Chromosome - C0008625 L0008626 S0009139 A0017829 M0004406 MeSH PM D002869 → |
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Abnormality, Congenital - C0000768 L0009679 S0009140 A0017830 M0000013 MeSH PM D000013 → |
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Abnormality, Congenital - C0000768 L0009679 S0009140 A0017830 M0000013 MeSH PM D000013 → |
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Abnormality, Craniofacial (MeSH) - C0376634 L0487001 S0583219 A0637492 M0028956 MeSH PM D019465 → |
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Abnormality, Cytogenetic - C0008625 L2300490 S2716669 A2362936 M0004406 MeSH PM D002869 → |
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Abnormality, Digestive System (MeSH) - C0266015 L0012241 S0793307 A0852593 M0006373 MeSH PM D004065 → |
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Abnormality, Drug-Induced - C0000771 L0000771 S0009141 A0017831 M0000014 MeSH PM D000014 → |
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Abnormality, Drug-Induced - C0000771 L0000771 S0009141 A0017831 M0000014 MeSH PM D000014 → |
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