| manager |
|
| language |
- |
| license |
- |
| 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"
|
82,788 entries
|
There is 0 pattern entry.
|
Mendelian Inheritance in Man [MIM] 604367
|
DISEASE |
|
|
mendelian inheritance in man [MIM] 604367
|
DISEASE |
|
|
congenital or infantile nephrotic syndrome
|
DISEASE |
|
|
hypoxic-ischemic (HI) injury
|
DISEASE |
|
|
hypoxic-ischemic neuronal injury
|
DISEASE |
|
|
congenital nuclear lactescent cataract
|
DISEASE |
|
|
Deficits in learning and memory
|
DISEASE |
|
|
longer QT interval
|
DISEASE |
|
|
prolonged QTc interval
|
DISEASE |
|
|
intraventricular and intracerebral haemorrhage
|
DISEASE |
|
|
reduction of mitochondrial complex III
|
DISEASE |
|
|
anterior segment malformation
|
DISEASE |
|
|
anterior segment malformations
|
DISEASE |
|
|
axial skeletal malformations
|
DISEASE |
|
|
deficits in learning and memory
|
DISEASE |
|
