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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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AEMK
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C1719788 |
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MYOKYMIA WITH PERIODIC ATAXIA
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C1719788 |
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Isaacs-Mertens syndrome
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C1719788 |
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myokymia 1
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C1719788 |
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familial paroxysmal kinesigenic ataxia and continuous myokymia
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C1719788 |
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Myokymia 1 With Or Without Hypomagnesemia
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C1719788 |
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acetazolamide-responsive periodic ataxia
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C1719788 |
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hereditary episodic ataxia caused by mutation in KCNA1
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C1719788 |
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hereditary paroxysmal ataxia with neuromyotonia
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C1719788 |
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KCNA1 hereditary episodic ataxia
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C1719788 |
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Myokymia with Periodic Ataxia
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C1719788 |
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EPISODIC ATAXIA, TYPE 1
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C1719788 |
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continuous muscle fiber activity
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C1719788 |
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continuous muscle fiber activity, hereditary
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C1719788 |
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continuous muscle fibre activity
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C1719788 |
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