All terms in MONDO
| Label |
Id |
Description |
|
mitral atresia disorder
|
MONDO_0015249 |
|
|
ataxia-photosensitivity-short stature syndrome
|
MONDO_0015248 |
|
|
opsoclonus-myoclonus syndrome
|
MONDO_0015247 |
|
|
neuronopathy, distal hereditary motor, type 5C
|
MONDO_0030860 |
|
|
arthrogryposis-like syndrome
|
MONDO_0015241 |
|
|
COACH syndrome 3
|
MONDO_0030862 |
|
|
osteogenesis imperfecta, type 21
|
MONDO_0030861 |
|
|
obsolete rare intestinal disease
|
MONDO_0015245 |
|
|
peeling skin syndrome 6
|
MONDO_0054852 |
|
|
obsolete aspergillosis
|
MONDO_0015242 |
|
|
ovarian dysgenesis 6
|
MONDO_0054850 |
|
|
epilepsy, familial adult myoclonic, 6
|
MONDO_0054846 |
|
|
developmental and epileptic encephalopathy 89
|
MONDO_0030856 |
|
|
developmental and epileptic encephalopathy, 66
|
MONDO_0054845 |
|
|
COACH syndrome 2
|
MONDO_0030859 |
|
|
pontocerebellar hypoplasia, type 1D
|
MONDO_0054844 |
|
|
immunodeficiency 75
|
MONDO_0030858 |
|
|
ciliary dyskinesia, primary, 38
|
MONDO_0054843 |
|
|
obsolete myxopapillary ependymoma
|
MONDO_0003267 |
|
|
neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities
|
MONDO_0030852 |
|
