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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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myopathy, centronuclear, autosomal dominant
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C4551952 |
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myotubular myopathy, autosomal dominant
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C4551952 |
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autosomal dominant centronuclear myopathy
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C4551952 |
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autosomal dominant centronuclear myopathy caused by mutation in MYF6
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C4551952 |
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DNM2-related centronuclear myopathy
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C4551952 |
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myopathy, centronuclear, type 3
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C4551952 |
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myopathy, centronuclear, type 1
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C4551952 |
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