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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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CMT2B
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C537989 |
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HMSN2B
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C537989 |
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CMT 2b
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C537989 |
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HMSN IIB
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C537989 |
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autosomal dominant (PSN) peripheral sensory neuropathy
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C537989 |
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axonal, type 2b charcot-marie-tooth disease
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C537989 |
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neuronal, type 2b charcot-marie-tooth disease
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C537989 |
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hereditary motor and sensory neuropathy 2 b (HMSN 2 b)
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C537989 |
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charcot-marie-tooth disease, autosomal dominant, type 2b
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C537989 |
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hereditary motor and sensory neuropathy IIB
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C537989 |
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charcot-marie-tooth disease, type 2b
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C537989 |
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charcot-marie-tooth disease, axonal, type 2b
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C537989 |
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type 2b charcot-marie-tooth disease
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C537989 |
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type 2b charcot-marie-tooth neuropathy
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C537989 |
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charcot-marie-tooth disease, neuronal, type 2b
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C537989 |
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