All terms in MONDO
| Label |
Id |
Description |
|
autosomal recessive myogenic arthrogryposis multiplex congenita
|
MONDO_0017892 |
|
|
classic dopamine transporter deficiency syndrome
|
MONDO_0054835 |
|
|
parkinsonism-dystonia, infantile
|
MONDO_0013150 |
|
|
spermatogenic failure 49
|
MONDO_0030868 |
|
|
thrombocytopenia 7
|
MONDO_0030867 |
|
|
charcot-marie-tooth disease, axonal, type 2DD
|
MONDO_0054833 |
|
|
corneal dystrophy, posterior polymorphous, 4
|
MONDO_0054832 |
|
|
spermatogenic failures 50
|
MONDO_0030869 |
|
|
neurohypophysis granular cell tumor
|
MONDO_0003256 |
|
|
Ritscher-Schinzel syndrome 3
|
MONDO_0030864 |
|
|
cardiomyopathy, familial hypertrophic 27
|
MONDO_0054838 |
|
|
intellectual disability, autosomal dominant 57
|
MONDO_0054837 |
|
|
hobnail hemangioma
|
MONDO_0003258 |
|
|
neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities
|
MONDO_0030866 |
|
|
parkinsonism-dystonia, infantile, 2
|
MONDO_0054836 |
|
|
obsolete melioidosis
|
MONDO_0003259 |
|
|
vulvar granular cell tumor
|
MONDO_0003253 |
|
|
cardiac granular cell neoplasm
|
MONDO_0003254 |
|
|
mediastinal granular cell myoblastoma
|
MONDO_0003255 |
|
|
esophageal granular cell tumor
|
MONDO_0003251 |
|
