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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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ARCA2
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C2677589 |
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COQ10D4
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C2677589 |
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SCAR9
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C2677589 |
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SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 9
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C2677589 |
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COENZYME Q10 DEFICIENCY, PRIMARY, 4
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C2677589 |
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Spinocerebellar Ataxia, Autosomal Recessive 9
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C2677589 |
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Cerebellar Ataxia, Autosomal Recessive, Type 2
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C2677589 |
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Autosomal recessive cerebellar ataxia type 2
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C2677589 |
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Autosomal recessive ataxia due to coenzyme Q10 deficiency
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C2677589 |
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autosomal recessive ataxia due to coenzyme Q10 deficiency
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C2677589 |
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Autosomal recessive ataxia due to ubiquinone deficiency
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C2677589 |
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autosomal recessive ataxia due to ubiquinone deficiency
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C2677589 |
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Spinocerebellar ataxia, autosomal recessive 9
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C2677589 |
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spinocerebellar ataxia, autosomal recessive 9
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C2677589 |
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ARCA2 - autosomal recessive cerebellar ataxia type 2
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C2677589 |
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