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
velocardiofacial syndrome D004062
deletion syndrome, 22q11.2 D004062
third and fourth pharyngeal pouch syndrome D004062
familial third and fourth pharyngeal pouch syndrome D004062
conotruncal anomaly face syndrome D004062
conotruncal anomaly face syndrome (CTAF) D004062
velo cardio facial syndrome D004062
hypoplasia of thymus and parathyroids D004062
autosomal dominant opitz g bbb syndrome D004062
autosomal dominant opitz g-bbb syndrome D004062
22q11.2 deletion syndrome D004062
deletion 22q11.2 syndrome D004062
pharyngeal pouch syndrome D004062
shprintzen VCF syndrome D004062
thymic aplasia syndrome D004062