Disease_Mesh_All (82,788) Find_IDs Annotation
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created at 2021-12-23 00:44:09 UTC
updated at 2021-12-23 01:31:33 UTC
"MeSH2022Disease.tsv"
"MeSH2022MentalDisorder.tsv"
"Addition_for_LitCoin_Disease.tsv"
"Addition_for_LitCoin_Disease_2.tsv"
Label
Id
deficiency of neutrophil cytosol factor 2 C565531
granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II C565531
granulomatous disease, chronic, due to NCF2 deficiency C565531
autosomal recessive cytochrome b-positive, type II CGD C565531
neutrophil cytosol factor 2, deficiency of C565531
p67-phox, deficiency of C565531
deficiency of p67-phox C565531
CGD, autosomal recessive cytochrome b-positive, type II C565531
chronic, autosomal recessive, cytochrome b-positive, type II granulomatous disease C565531
chronic, due to NCF2 deficiency granulomatous disease C565531