All terms in MONDO
| Label |
Id |
Description |
|
obsolete facial paresis, hereditary congenital
|
MONDO_0000122 |
|
|
hemangiopericytic tumor
|
MONDO_0002789 |
|
|
obsolete emphysema
|
MONDO_0000121 |
|
|
Shwartzman phenomenon
|
MONDO_0002783 |
|
|
vascular hemostatic disease
|
MONDO_0003159 |
|
|
giant axonal neuropathy
|
MONDO_0000128 |
|
|
geleophysic dysplasia
|
MONDO_0000127 |
|
|
obsolete craniopharyngioma
|
MONDO_0002784 |
|
|
obsolete gastric cancer
|
MONDO_0000126 |
|
|
obsolete fundus dystrophy, pseudoinflammatory
|
MONDO_0000125 |
|
|
obsolete MONDO:0002780
|
MONDO_0002780 |
|
|
glossopharyngeal nerve paralysis
|
MONDO_0002781 |
|
|
intellectual disability, autosomal recessive 51
|
MONDO_0014759 |
|
|
obsolete ectopia lentis, isolated
|
MONDO_0000120 |
|
|
epilepsy, idiopathic generalized, susceptibility to, 3
|
MONDO_0012113 |
|
|
spinocerebellar ataxia type 42
|
MONDO_0014776 |
|
|
combined oxidative phosphorylation deficiency 28
|
MONDO_0014775 |
|
|
Ehlers-Danlos syndrome, Beasley-Cohen type
|
MONDO_0012114 |
|
|
neuroblastoma, susceptibility to, 7
|
MONDO_0014774 |
|
|
hypertrophic cardiomyopathy 8
|
MONDO_0012111 |
|
