|
primary immunodeficiency disease
|
3778 |
|
|
immune deficiency disorder
|
3778 |
|
|
blood coagulation disorders
|
D001778 |
|
|
aortic aneurysm-aortic dissection and patent ductus arteriosus
|
C537784 |
|
|
Charcot-Marie-Tooth disease dominant intermediate
|
http://purl.obolibrary.org/obo/MONDO_0018778 |
|
|
hyperthyroidism, familial, due to inappropriate thyrotropin secretion
|
7784 |
|
|
multiple epiphyseal dysplasia, Al-Gazali type
|
11778 |
|
|
multiple epiphyseal dysplasia-macrocephaly-distinctive facies syndrome
|
11778 |
|
|
aipl1-related cone-rod dystrophy
|
C565778 |
|
|
lattice corneal dystrophy type ii
|
C000657784 |
|
|
lattice corneal dystrophy, gelsolin type
|
C000657784 |
|
|
lattice corneal dystrophy, type II
|
C000657784 |
|
|
meningioma of epidural spinal canal
|
2778 |
|
|
Leiner-Moussous desquamative erythroderma
|
17787 |
|
|
malaria, plasmodium falciparum
|
D016778 |
|
