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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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Wadia Swami Syndrome
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C0752121 |
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Atrophy 2, Olivopontocerebellar
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C0752121 |
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Atrophy 2s, Olivopontocerebellar
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C0752121 |
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Atrophy II, Olivopontocerebellar
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C0752121 |
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CEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS
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C0752121 |
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SPINOCEREBELLAR DEGENERATION WITH SLOW EYE MOVEMENTS
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C0752121 |
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Swami Syndrome, Wadia
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C0752121 |
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Wadia Swami syndrome
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C0752121 |
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amyotrophic lateral sclerosis 13
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C0752121 |
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amyotrophic lateral sclerosis type 13
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C0752121 |
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autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2
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C0752121 |
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ATXN2 autosomal dominant cerebellar ataxia type I
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C0752121 |
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amyotrophic lateral sclerosis, susceptibility to, 13
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C0752121 |
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Wadia swami syndrome
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C0752121 |
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Spinocerebellar ataxia type 2
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C0752121 |
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