|
chromosome abnormality disorders
|
19040 |
|
|
chromosome Abnormality disorders
|
http://purl.obolibrary.org/obo/MONDO_0019040 |
|
|
mannosidase deficiency diseases
|
D044904 |
|
|
autosomal chromosome disorder
|
19040 |
|
|
chromosome abnormality disorder
|
19040 |
|
|
chromosome Abnormality disorder
|
http://purl.obolibrary.org/obo/MONDO_0019040 |
|
|
mannosidase deficiency disease
|
D044904 |
|
|
isolated, autosomal dominant, 1 preauricular tag
|
C566904 |
|
|
Cushing syndrome due to macronodular adrenal hyperplasia
|
9049 |
|
|
progressive myoclonic epilepsy caused by mutation in PRICKLE1
|
12904 |
|
|
POMGNT2 muscular dystrophy-dystroglycanopathy, type A
|
13904 |
|
|
seizures, benign familial neonatal-infantile
|
11904 |
|
|
Baraitser Rodeck garner syndrome
|
9041 |
|
