| 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.
|
cardiovascular, craniofacial, and thymic malformations
|
DISEASE |
|
|
multiple cutaneous and uterine leiomyomas
|
DISEASE |
|
|
necrosis and apoptosis of tubular cells
|
DISEASE |
|
|
axial and appendicular skeletal malformation
|
DISEASE |
|
|
loss of appetite
|
DISEASE |
|
|
calcification of ascending aorta
|
DISEASE |
|
|
deficits in auditory discrimination
|
DISEASE |
|
|
impairment in auditory discrimination
|
DISEASE |
|
|
impairment in auditory location discrimination
|
DISEASE |
|
|
jaw of steel
|
DISEASE |
|
|
type I congenital antithrombin deficiency
|
DISEASE |
|
|
type i congenital antithrombin deficiency
|
DISEASE |
|
|
autosomal dominant congenital nuclear cataract
|
DISEASE |
|
|
autosomal dominant congenital nuclear lactescent cataract
|
DISEASE |
|
|
Scleroderma renal crisis
|
DISEASE |
|