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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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3MC1
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C0796059 |
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craniosynostosis with 51D anomalies
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C0796059 |
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3MC1 syndrome
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C0796059 |
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Michels syndrome
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C0796059 |
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OCULOPALATOSKELETAL SYNDROME
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C0796059 |
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Oculopalatoskeletal syndrome
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C0796059 |
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oculopalatoskeletal syndrome
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C0796059 |
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3MC SYNDROME 1
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C0796059 |
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3MC syndrome 1
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C0796059 |
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CRANIOSYNOSTOSIS WITH LID ANOMALIES
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C0796059 |
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MICHELS SYNDROME, FORMERLY
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C0796059 |
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Craniosynostosis with lid anomalies
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C0796059 |
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3MC syndrome caused by mutation in MASP1
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C0796059 |
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Michels syndrome, formerly
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C0796059 |
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MASP1 3MC syndrome
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C0796059 |
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