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
CMT2A2 C563757
HMSN2A2 C563757
HMSNIIA2 C563757
hereditary motor and sensory neuropathy IIA2 C563757
axonal, type 2a2 charcot-marie-tooth disease C563757
neuronal, type 2a2 charcot-marie-tooth disease C563757
type 2a2 charcot-marie-tooth neuropathy C563757
charcot-marie-tooth disease, axonal, autosomal dominant, type 2a2 C563757
charcot-marie-tooth disease, axonal, type 2a2 C563757
axonal, autosomal dominant, type 2a2 charcot-marie-tooth disease C563757
charcot-marie-tooth disease, neuronal, type 2a2 C563757
charcot-marie-tooth neuropathy, type 2a2 C563757
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