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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.
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AI1H
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C4015557 |
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amelogenesis imperfecta caused by mutation in ITGB6
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C4015557 |
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Amelogenesis imperfecta type 1H
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C4015557 |
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amelogenesis imperfecta type 1H
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C4015557 |
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amelogenesis imperfecta, type 1H
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C4015557 |
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AMELOGENESIS IMPERFECTA, TYPE IH
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C4015557 |
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ITGB6 amelogenesis imperfecta
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C4015557 |
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Amelogenesis imperfecta, type IH
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C4015557 |
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amelogenesis imperfecta type IH
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C4015557 |
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amelogenesis imperfecta, type IH
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C4015557 |
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