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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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ADHCAI
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CN377797 |
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AI3A
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CN377797 |
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amelogenesis imperfecta caused by mutation in FAM83H
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CN377797 |
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AMELOGENESIS IMPERFECTA, TYPE IIIA
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CN377797 |
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AMELOGENESIS IMPERFECTA, TYPE IIIA, LOCALIZED
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CN377797 |
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autosomal dominant amelogenesis imperfecta hypocalcification type
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CN377797 |
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amelogenesis imperfecta, hypocalcification type, autosomal dominant
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CN377797 |
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amelogenesis imperfecta, hypomineralization type
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CN377797 |
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amelogenesis imperfecta, type III
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CN377797 |
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FAM83H amelogenesis imperfecta
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CN377797 |
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amelogenesis imperfecta, type 3
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CN377797 |
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Amelogenesis imperfecta, type 3A
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CN377797 |
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amelogenesis imperfecta type 3A
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CN377797 |
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amelogenesis imperfecta, type 3A
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CN377797 |
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amelogenesis imperfecta, type IIIA
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CN377797 |
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