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
cerebroocular dysplasia-muscular dystrophy syndrome D058494
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type a1 D058494
walker-warburg syndrome, fktn-related D058494
muscular dystrophy, fukuyama D058494
cerebromuscular dystrophy, fukuyama type D058494
muscular dystrophy, limb-girdle, autosomal recessive, with mental retardation D058494
muscular dystrophy, limb-girdle, type 2k D058494
POMT1 related muscle eye brain disease D058494
disease, POMT1-Related muscle-eye-brain D058494
dystrophy, fukuyama muscular D058494
fukuyama congenital muscular dystrophy D058494
cerebroocular dysplasia muscular dystrophy syndrome D058494
limb-girdle, autosomal recessive, with mental retardation muscular dystrophy D058494
agyria, and retinal dysplasia hydrocephalus D058494
COD MD syndrome D058494