|
pituitary hormone deficiency, combined, 2
|
9878 |
|
|
pituitary hormone deficiency, combined, 2; CPHD2
|
http://purl.obolibrary.org/obo/MONDO_0009878 |
|
|
pituitary hormone deficiency, combined, type 2
|
9878 |
|
|
erythrocyte amp deaminase deficiency
|
C567878 |
|
|
Moraxellaceae infectious disease
|
6878 |
|
|
familial high density lipoprotein deficiency
|
8783 |
|
|
Alpha high density lipoprotein deficiency disease
|
8783 |
|
|
familial high density lipoprotein deficiency disease
|
8783 |
|
|
constitutional liver dysfunction
|
D005878 |
|
|
Moraxellaceae caused disease or disorder
|
6878 |
|
|
Van Buchem disease type 2
|
11878 |
|
|
obsolete rare disease with autism
|
15878.0 |
|
|
Van Buchem disease, type 2
|
11878 |
|
|
ichthyosis oligophrenia epilepsy syndrome
|
C535878 |
|
|
neonatal severe, due to mecp2 mutations encephalopathy
|
C566878 |
|
