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created at |
2024-09-19 07:43:07 UTC |
updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
AI1G
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C2931783 |
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AIGFS
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C2931783 |
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ers
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C2931783 |
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AMELOGENESIS IMPERFECTA, HYPOPLASTIC, AND NEPHROCALCINOSIS
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C2931783 |
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ENAMEL-RENAL SYNDROME
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C2931783 |
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ENAMEL-RENAL-GINGIVAL SYNDROME
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C2931783 |
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Enamel-Renal Syndrome
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C2931783 |
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Enamel-renal syndrome
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C2931783 |
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enamel-renal syndrome
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C2931783 |
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enamel-renal-gingival syndrome
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C2931783 |
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AMELOGENESIS IMPERFECTA AND GINGIVAL FIBROMATOSIS SYNDROME
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C2931783 |
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AMELOGENESIS IMPERFECTA, HYPOPLASTIC, WITH NEPHROCALCINOSIS
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C2931783 |
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Amelogenesis Imperfecta, Hypoplastic, and Nephrocalcinosis
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C2931783 |
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Amelogenesis imperfecta-gingival hyperplasia syndrome
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C2931783 |
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Amelogenesis Imperfecta, Type IG
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C2931783 |
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