|
pseudohermaphroditism, male internal
|
C536665 |
|
|
synergistic divergence, jaw winking, and oculocutaneous hypopigmentation external ophthalmoplegia
|
C566509 |
|
|
juvenile amyotrophic lateral sclerosis 4
|
C566550 |
|
|
autosomal dominant lewy body parkinson disease 3
|
C566552 |
|
|
familial pancreatic lymphoma
|
C566516 |
|
|
muscular dystrophy, limb-girdle, type 1e
|
C566589 |
|
|
muscular dystrophy, limb-girdle, type 2g
|
C566599 |
|
|
classical Hodgkin lymphoma, nodular sclerosis
|
4665 |
|
|
colobomatous, with microcornea macrophthalmia
|
C566533 |
|
|
high grade malignant neoplasm
|
20665 |
|
|
benign familial microcytic thrombocytosis
|
C566596 |
|
|
familial basilar migraine
|
C566540 |
|
|
epilepsy, juvenile myoclonic, susceptibility to, 9
|
13665 |
|
|
epilepsy, juvenile myoclonic, susceptibility to, 9; EJM9
|
http://purl.obolibrary.org/obo/MONDO_0013665 |
|
