|
EORTC GIMEMA AML-13 protocol
|
C521113 |
|
|
NUP214-ABL1 fusion protein, human
|
C521114 |
|
|
HLA-DRB1*02 antigen
|
C521115 |
|
|
KLHDC1 protein, human
|
C521116 |
|
|
LDP-4 protein, mouse
|
C521117 |
|
|
p-imazamethabenz-methyl
|
C521118 |
|
|
GLUD2 protein, human
|
C521120 |
|
|
Congenital disorder of glycosylation type 2A
|
C535752 |
|
|
Congenital disorder of glycosylation type 2D
|
C535753 |
|
|
Congenital disorder of glycosylation type 2E
|
C535754 |
|
|
Congenital disorder of glycosylation, type 2C
|
C535755 |
|
|
Congenital disorder of glycosylation, type 2G
|
C535756 |
|
|
Congenital ectodermal dysplasia with hearing loss
|
C535757 |
|
|
Congenital heart block
|
C535758 |
|
|
Congenital myasthenic syndrome with episodic apnea
|
C535759 |
|
|
Chitayat Moore Del Bigio syndrome
|
C535927 |
|
|
Chitty Hall Baraitser syndrome
|
C535928 |
|
|
Chitty Hall Webb syndrome
|
C535929 |
|
|
Cheilitis glandularis
|
C535921 |
|
|
Chemke Oliver Mallek syndrome
|
C535922 |
|
