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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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Spinocerebellar Ataxia Type 7
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C0752125 |
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Autosomal dominant cerebellar ataxia type 2
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C0752125 |
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autosomal dominant cerebellar ataxia type 2
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C0752125 |
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Autosomal dominant cerebellar ataxia type II
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C0752125 |
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autosomal dominant cerebellar ataxia type II
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C0752125 |
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autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7
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C0752125 |
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autosomal dominant cerebellar ataxia, type 2
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C0752125 |
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ATXN7 autosomal dominant cerebellar ataxia type II
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C0752125 |
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OPCA with macular Degeneration and external ophthalmoplegia
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C0752125 |
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cerebellar syndrome-pigmentary maculopathy syndrome
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C0752125 |
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Cerebellar syndrome pigmentary maculopathy
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C0752125 |
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Ataxia with pigmentary retinopathy
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C0752125 |
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ataxia with pigmentary retinopathy
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C0752125 |
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OPCA with retinal Degeneration
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C0752125 |
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Spinocerebellar ataxia type 7
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C0752125 |
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