| 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.
|
cerebellar hypoplasia, nonprogressive norman type
|
C565865 |
|
|
CPD3
|
C565865 |
|
|
SCAR2
|
C565865 |
|
|
CPD III
|
C565865 |
|
|
autosomal recessive 2 spinocerebellar ataxia
|
C565865 |
|
|
cerebelloparenchymal disorder III
|
C565865 |
|
|
spinocerebellar ataxia autosomal recessive 2
|
C565865 |
|
|
spinocerebellar ataxia, autosomal recessive 2
|
C565865 |
|
|
congenital cerebellar granular cell hypoplasia and mental retardation
|
C565865 |
|
|
cerebellar granular cell hypoplasia and mental retardation, congenital
|
C565865 |
|
|
nonprogressive norman type cerebellar hypoplasia
|
C565865 |
|
