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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 and gingival fibromatosis syndrome
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C2931783 |
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amelogenesis imperfecta and gingival fibromatosis syndrome
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C2931783 |
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Amelogenesis imperfecta and nephrocalcinosis
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C2931783 |
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amelogenesis imperfecta and nephrocalcinosis
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C2931783 |
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amelogenesis imperfecta caused by mutation in FAM20A
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C2931783 |
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Amelogenesis imperfecta-gingival hyperplasia syndrome
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C2931783 |
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amelogenesis imperfecta-gingival hyperplasia syndrome
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C2931783 |
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Generalized enamel hypoplasia and renal dysfunction
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C2931783 |
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generalised enamel hypoplasia and renal dysfunction
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C2931783 |
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generalized enamel hypoplasia and renal dysfunction
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C2931783 |
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Amelogenesis imperfecta hypoplastic type, IG
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C2931783 |
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amelogenesis imperfecta hypoplastic type, IG
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C2931783 |
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amelogenesis imperfecta hypoplastic with nephrocalcinosis
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C2931783 |
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amelogenesis imperfecta, hypoplastic, with nephrocalcinosis
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C2931783 |
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FAM20A amelogenesis imperfecta
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C2931783 |
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