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
CMT2A1 C566138
HMSN2A1 C566138
HMSN IIA1 C566138
charcot-marie-tooth disease, axonal, autosomal dominant, type 2a1 C566138
axonal, type 2a1 charcot-marie-tooth disease C566138
neuronal, type 2a1 charcot-marie-tooth disease C566138
charcot-marie-tooth disease, axonal, type 2a1 C566138
type 2a1 charcot-marie-tooth neuropathy C566138
hereditary motor and sensory neuropathy IIA1 C566138
charcot-marie-tooth neuropathy, type 2a1 C566138
axonal, autosomal dominant, type 2a1 charcot-marie-tooth disease C566138
charcot-marie-tooth disease, neuronal, type 2a1 C566138