All terms in MONDO
| Label |
Id |
Description |
|
obsolete hyperprolinemia
|
MONDO_0000042 |
|
|
obsolete hyperphosphatasia with mental retardation syndrome
|
MONDO_0000041 |
|
|
obsolete hyperphenylalaninemia, BH4-deficient
|
MONDO_0000040 |
|
|
systemic lupus erythematosus, susceptibility to, 4
|
MONDO_0012036 |
|
|
intellectual disability, autosomal dominant 40
|
MONDO_0014699 |
|
|
microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome
|
MONDO_0014698 |
|
|
intellectual disability, autosomal recessive 3
|
MONDO_0012037 |
|
|
immunodeficiency, common variable, 12
|
MONDO_0014697 |
|
|
autosomal dominant limb-girdle muscular dystrophy type 1F
|
MONDO_0012034 |
|
|
craniosynostosis-intracranial calcifications syndrome
|
MONDO_0012035 |
|
|
cerebrooculofacioskeletal syndrome 3
|
MONDO_0014696 |
|
|
speech-sound disorder
|
MONDO_0012038 |
|
|
myocardial infarction, susceptibility to
|
MONDO_0012039 |
|
|
Noonan syndrome 9
|
MONDO_0014691 |
|
|
dyskeratosis congenita, autosomal dominant 6
|
MONDO_0014690 |
|
|
glioma susceptibility 9
|
MONDO_0014695 |
|
|
Braddock syndrome
|
MONDO_0012032 |
|
|
bradyopsia
|
MONDO_0012033 |
|
|
spondylocostal dysostosis 6, autosomal recessive
|
MONDO_0014694 |
|
|
Noonan syndrome 10
|
MONDO_0014693 |
|
