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
Label
Id
CMT2C C565261
HMSN2C C565261
type IIC hereditary motor and sensory neuropathy C565261
axonal, autosomal dominant, type 2c charcot-marie-tooth disease C565261
HMSN IIC C565261
hereditary motor and sensory neuropathy, type IIC C565261
type 2c charcot-marie-tooth neuropathy C565261
charcot-marie-tooth disease, axonal, autosomal dominant, type 2c C565261
charcot-marie-tooth neuropathy, type 2c C565261