All terms in MONDO
| Label |
Id |
Description |
|
cardiomyopathy, dilated, 2H
|
MONDO_0859358 |
|
|
obsolete rare tumor of salivary glands
|
MONDO_0017166 |
|
|
congenital hypotonia, epilepsy, developmental delay, and digital anomalies
|
MONDO_0032781 |
|
|
spermatogenic failure 79
|
MONDO_0859352 |
|
|
ciliary dyskinesia, primary, 49, without situs inversus
|
MONDO_0859353 |
|
|
thyroid hormone metabolism, abnormal, 3
|
MONDO_0859354 |
|
|
imperforate oropharynx-costo vetebral anomalies syndrome
|
MONDO_0017162 |
|
|
neurodevelopmental disorder with microcephaly and structural brain anomalies
|
MONDO_0032779 |
|
|
silver-russell syndrome 2
|
MONDO_0030116 |
|
|
silver-russell syndrome 4
|
MONDO_0030118 |
|
|
generalized epilepsy with febrile seizures plus, type 10
|
MONDO_0032777 |
|
|
neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies
|
MONDO_0859350 |
|
|
arthrogryposis multiplex congenita 3, myogenic type
|
MONDO_0032778 |
|
|
obesity and hypopigmentation
|
MONDO_0859351 |
|
|
lumbar spinal stenosis
|
MONDO_0044753 |
|
|
spinal stenosis
|
MONDO_0005965 |
|
|
internal carotid artery stenosis
|
MONDO_0005189 |
|
|
severe combined immunodeficiency due to CARMIL2 deficiency
|
MONDO_0029134 |
|
|
muscular dystrophy, limb-girdle, autosomal dominant 4
|
MONDO_0029133 |
|
|
iatrogenic Kaposi's sarcoma
|
MONDO_0005188 |
|
