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| language |
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| license |
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| created at |
2021-12-23 00:44:09 UTC |
| updated at |
2021-12-23 01:31:33 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,788 entries
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There is 0 pattern entry.
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spinal muscular atrophy, oculopharyngeal
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D009134 |
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myelopathic muscular atrophy, progressive
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D009134 |
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spinal muscular atrophy, scapuloperoneal
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D009134 |
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spinal muscular atrophy, scapuloperoneal form
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D009134 |
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motor neuronopathies, hereditary
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D009134 |
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motor neuronopathy, hereditary
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D009134 |
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hereditary motor neuronopathies
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D009134 |
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hereditary motor neuronopathy
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D009134 |
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scapuloperoneal form of spinal muscular atrophy
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D009134 |
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amyotrophy, neurogenic scapuloperoneal, new england type
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D009134 |
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muscular atrophies, progressive
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D009134 |
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muscular atrophy, progressive
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D009134 |
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neuronopathies, hereditary motor
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D009134 |
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neuronopathy, hereditary motor
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D009134 |
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atrophies, progressive muscular
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D009134 |
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