| manager |
|
| language |
- |
| license |
- |
| 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.
|
familial defective apolipoprotein b 100
|
D006938 |
|
|
familial defective apolipoprotein b-100
|
D006938 |
|
|
familial ligand-defective apolipoprotein b-100
|
D006938 |
|
|
dominant hypercholesterolemia, autosomal
|
D006938 |
|
|
dominant hypercholesterolemias, autosomal
|
D006938 |
|
|
hyperlipoproteinemia, familial combined
|
D006938 |
|
|
hyperlipoproteinemias, familial combined
|
D006938 |
|
|
familial ligand defective apolipoprotein b 100
|
D006938 |
|
|
lipoproteinemia, hyper-low density
|
D006938 |
|
|
lipoproteinemias, hyper-low density
|
D006938 |
|
|
hyper low density lipoproteinemia
|
D006938 |
|
|
LDL receptor disorder
|
D006938 |
|
|
LDL receptor disorders
|
D006938 |
|
|
hypercholesterolemia, autosomal dominant
|
D006938 |
|
|
hypercholesterolemias, autosomal dominant
|
D006938 |
|
