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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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AIHHT
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C1863012 |
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AMELOGENESIS IMPERFECTA, HYPOMATURATION-HYPOPLASTIC TYPE, WITH TAURODONTISM
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C1863012 |
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amelogenesis imperfecta caused by mutation in DLX3
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C1863012 |
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Amelogenesis Imperfecta, Hypomaturation-Hypoplastic Type, with Taurodontism
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C1863012 |
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AMELOGENESIS IMPERFECTA, TYPE IV
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C1863012 |
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amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism
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C1863012 |
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amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism
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C1863012 |
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Amelogenesis Imperfecta, Type IV
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C1863012 |
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DLX3 amelogenesis imperfecta
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C1863012 |
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Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
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C1863012 |
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hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
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C1863012 |
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Amelogenesis imperfecta type 4
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C1863012 |
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amelogenesis imperfecta type 4
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C1863012 |
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amelogenesis imperfecta, type 4
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C1863012 |
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Amelogenesis imperfecta, type IV
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C1863012 |
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