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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
muscular, peroneal atrophy D002607
peroneal muscular atrophy D002607
charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a D002607
charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1b D002607
type 1a charcot marie tooth disease D002607
type 1b charcot marie tooth disease D002607
type IA charcot marie tooth disease D002607
type IB charcot marie tooth disease D002607
type II charcot marie tooth disease D002607
type i charcot marie tooth disease D002607
type 1a charcot marie tooth neuropathy D002607
type 1b charcot marie tooth neuropathy D002607
hereditary neuropathy, charcot-marie-tooth D002607
type 1a charcot-marie-tooth disease D002607
type 1b charcot-marie-tooth disease D002607
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