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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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AI2A1
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C2673922 |
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Ai2a1
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C2673922 |
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amelogenesis imperfecta caused by mutation in KLK4
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C2673922 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION TYPE, IIA1
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C2673922 |
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AMELOGENESIS IMPERFECTA, PIGMENTED HYPOMATURATION TYPE, 1
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C2673922 |
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Amelogenesis Imperfecta, Hypomaturation Type, Iia1
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C2673922 |
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Amelogenesis Imperfecta, Pigmented Hypomaturation Type, 1
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C2673922 |
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Amelogenesis imperfecta, hypomaturation type, IIA1
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C2673922 |
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amelogenesis imperfecta, hypomaturation type, IIA1
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C2673922 |
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Amelogenesis imperfecta, type IIA1
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C2673922 |
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amelogenesis imperfecta pigmented hypomaturation type
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C2673922 |
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amelogenesis imperfecta pigmented hypomaturation type 1
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C2673922 |
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amelogenesis imperfecta, pigmented hypomaturation type, 1
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C2673922 |
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Amelogenesis imperfecta type 2A1
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C2673922 |
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amelogenesis imperfecta type 2A1
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C2673922 |
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