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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.
demyelinating, type 1a charcot-marie-tooth disease
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D002607 |
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demyelinating, type 1b charcot-marie-tooth disease
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D002607 |
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hereditary motor and sensory neuropathy 1a
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D002607 |
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HMSN type II
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D002607 |
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neuropathy, type II hereditary motor and sensory
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D002607 |
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hereditary motor and sensory neuropathy 1b
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D002607 |
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hereditary motor and sensory neuropathy IA
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D002607 |
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hereditary motor and sensory neuropathy IB
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D002607 |
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hereditary motor and sensory neuropathy type II
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D002607 |
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hereditary motor, and sensory neuropathy type i
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D002607 |
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hereditary motor and sensory-neuropathy type II
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D002607 |
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dystasia, hereditary areflexic
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D002607 |
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peroneal muscular atrophies
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D002607 |
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muscular, peroneal atrophy
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D002607 |
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peroneal muscular atrophy
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D002607 |
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