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| created at |
2021-12-22 03:08:20 UTC |
| updated at |
2021-12-22 07:06:09 UTC |
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MONDO_bioport_pref_name
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183,974 entries
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There is 0 pattern entry.
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spinocerebellar atrophy 2
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8458 |
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spinocerebellar ataxia 2; SCA2
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http://purl.obolibrary.org/obo/MONDO_0008458 |
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spinocerebellar ataxia Cuban type
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8458 |
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spinocerebellar ataxia, Cuban type
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8458 |
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olivopontocerebellar atrophy Holguin type
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8458 |
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olivopontocerebellar atrophy, Holguin type
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8458 |
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autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2
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8458 |
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state, minimally conscious
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D018458 |
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states, minimally conscious
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D018458 |
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ATXN2 autosomal dominant cerebellar ataxia type I
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8458 |
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familial benign hypercalcemia
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18458 |
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familial hypocalciuric hypercalcemia
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18458 |
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familial benign hypocalciuric hypercalcemia
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18458 |
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Anti-glomerular basement membrane antibody disease
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C538458 |
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vegetative state, permanent
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D018458 |
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