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
HMN2A C563561
HMN IIA C563561
spinal muscular atrophy, distal adult autosomal dominant, IIA C563561
distal adult autosomal dominant, IIA spinal muscular atrophy C563561
spinal, IIA charcot-marie-tooth disease C563561
neuronopathy, distal hereditary motor, type IIA C563561
neuropathy, distal hereditary motor, type IIA C563561
charcot-marie-tooth disease, spinal, IIA C563561
distal hereditary motor, type IIA neuronopathy C563561
distal hereditary motor, type IIA neuropathy C563561