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| language |
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| license |
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| created at |
2021-12-23 02:14:06 UTC |
| updated at |
2021-12-23 14:43:01 UTC |
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"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
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82,725 entries
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There is 0 pattern entry.
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HMN2A
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C563561 |
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HMN IIA
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C563561 |
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spinal muscular atrophy, distal adult autosomal dominant, IIA
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C563561 |
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distal adult autosomal dominant, IIA spinal muscular atrophy
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C563561 |
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spinal, IIA charcot-marie-tooth disease
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C563561 |
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neuronopathy, distal hereditary motor, type IIA
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C563561 |
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neuropathy, distal hereditary motor, type IIA
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C563561 |
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charcot-marie-tooth disease, spinal, IIA
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C563561 |
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distal hereditary motor, type IIA neuronopathy
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C563561 |
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distal hereditary motor, type IIA neuropathy
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C563561 |
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