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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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AI1B
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C0399368 |
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AIH2
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C0399368 |
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Amelogenesis imperfecta - hypoplastic autosomal dominant - local
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C0399368 |
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ENAMEL HYPOPLASIA, HEREDITARY LOCALIZED
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C0399368 |
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AMELOGENESIS IMPERFECTA, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT
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C0399368 |
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Enamel Hypoplasia, Hereditary Localized
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C0399368 |
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Amelogenesis Imperfecta, Hypoplastic Local, Autosomal Dominant
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C0399368 |
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AMELOGENESIS IMPERFECTA, TYPE IB
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C0399368 |
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Amelogenesis Imperfecta, Type IB
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C0399368 |
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amelogenesis imperfecta caused by mutation in ENAM
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C0399368 |
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amelogenesis imperfecta caused by mutation in enam
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C0399368 |
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hereditary localised enamel hypoplasia
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C0399368 |
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hereditary localized enamel hypoplasia
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C0399368 |
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enamel hypoplasia, hereditary localised
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C0399368 |
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enamel hypoplasia, hereditary localized
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C0399368 |
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