Mesh_All_FN Find_IDs Find_Terms Annotation
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created at 2021-12-23 02:14:06 UTC
updated at 2021-12-23 14:43:01 UTC
"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
82,725 entries

There is 0 pattern entry.

Label
Id
demyelinating, type 1a charcot-marie-tooth disease D002607
demyelinating, type 1b charcot-marie-tooth disease D002607
HMSN type II D002607
neuropathy, type II hereditary motor and sensory D002607
peroneal muscular atrophies D002607
hereditary motor and sensory neuropathy 1a D002607
hereditary motor and sensory neuropathy 1b D002607
hereditary motor and sensory neuropathy IA D002607
hereditary motor and sensory neuropathy IB D002607
hereditary motor and sensory neuropathy type II D002607
hereditary motor, and sensory neuropathy type i D002607
hereditary motor and sensory-neuropathy type II D002607
muscular, peroneal atrophy D002607
peroneal muscular atrophy D002607
charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a D002607
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