|
type io congenital disorder of glycosylation
|
C567857 |
|
|
erythrocyte amp deaminase deficiency
|
C567878 |
|
|
chromosome 9p24.3 deletion syndrome
|
C567887 |
|
|
growth retardation, developmental delay, coarse facies, and early death
|
C567856 |
|
|
insulin-dependent, 24 diabetes mellitus
|
C567818 |
|
|
myelinosis centralis diffusas
|
D056784 |
|
|
glycogen storage disease IXC
|
C567809 |
|
|
glycogen storage disease XIV
|
C567859 |
|
|
bovine respiratory disease complex
|
5678 |
|
|
46,xy gonadal dysgenesis, complete or partial, with 9p24.3 deletion
|
C567887 |
|
|
emery-dreifuss muscular dystrophy 4
|
C567831 |
|
|
emery-dreifuss muscular dystrophy 4, autosomal dominant
|
C567831 |
|
|
emery-dreifuss muscular dystrophy 5
|
C567830 |
|
