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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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amelogenesis imperfecta X-linked 1
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C1845053 |
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amelogenesis imperfecta, X-linked 1
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C1845053 |
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amelogenesis imperfecta caused by mutation in AMELX
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C1845053 |
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X-linked enamel hypoplasia
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C1845053 |
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amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1
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C1845053 |
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amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1
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C1845053 |
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X-linked amelogenesis imperfecta 1
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C1845053 |
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X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1
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C1845053 |
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amelogenesis imperfecta type IE
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C1845053 |
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Amelogenesis imperfecta type 1E
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C1845053 |
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amelogenesis imperfecta type 1E
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C1845053 |
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amelogenesis imperfecta, type 1E
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C1845053 |
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amelogenesis imperfecta, type 1E, X-linked dominant
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C1845053 |
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amelogenesis imperfecta, type IE
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C1845053 |
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