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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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AI2A2
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C2675858 |
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Ai2a2
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C2675858 |
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Amelogenesis Imperfecta, Pigmented Hypomaturation Type, 2
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C2675858 |
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Amelogenesis Imperfecta, Hypomaturation Type, Iia2
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C2675858 |
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AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 2
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C2675858 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA2
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C2675858 |
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amelogenesis imperfecta caused by mutation in MMP20
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C2675858 |
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amelogenesis imperfecta pigmented hypomaturation type 2
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C2675858 |
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Amelogenesis imperfecta hypomaturation type 2A2
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C2675858 |
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amelogenesis imperfecta hypomaturation type 2A2
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C2675858 |
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amelogenesis imperfecta hypomaturation type IIA2
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C2675858 |
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Amelogenesis imperfecta, hypomaturation type, IIA2
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C2675858 |
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amelogenesis imperfecta, hypomaturation type, IIA2
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C2675858 |
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MMP20 amelogenesis imperfecta
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C2675858 |
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amelogenesis imperfecta, pigmented hypomaturation type, 2
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C2675858 |
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