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.
ARCL2A
|
C562632 |
|
cutis laxa with bone dystrophy
|
C562632 |
|
debre type cutis laxa
|
C562632 |
|
cutis laxa, debre type
|
C562632 |
|
cutis laxa, autosomal recessive, type IIA
|
C562632 |
|
autosomal recessive, type IIA cutis laxa
|
C562632 |
|
cutis laxa with growth and developmental delay
|
C562632 |
|
cutis laxa with or without congenital disorder of glycosylation
|
C562632 |
|
cutis laxa with joint laxity and retarded development
|
C562632 |
|