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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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ARAN-NM
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C5700127 |
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ARCMT2-NM
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C5700127 |
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NMAN
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C5700127 |
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Myokymia, myotonia and muscle wasting
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C5700127 |
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GAMSTORP-WOHLFART SYNDROME
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C5700127 |
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Gamstorp-Wohlfart syndrome
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C5700127 |
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MYOKYMIA, MYOTONIA, AND MUSCLE WASTING
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C5700127 |
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NEUROMYOTONIA AND AXONAL NEUROPATHY, AUTOSOMAL RECESSIVE
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C5700127 |
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Autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
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C5700127 |
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autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia
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C5700127 |
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myokymia, myotonia and muscle wasting
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C5700127 |
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myokymia, myotonia, and muscle wasting
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C5700127 |
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Autosomal recessive axonal neuropathy with neuromyotonia
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C5700127 |
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autosomal recessive axonal neuropathy with neuromyotonia
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C5700127 |
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Neuromyotonia and axonal neuropathy, autosomal recessive
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C5700127 |
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