All terms in MONDO
| Label |
Id |
Description |
|
microcephaly, growth deficiency, seizures, and brain malformations
|
MONDO_0032690 |
|
|
Galloway-Mowat syndrome 6
|
MONDO_0032691 |
|
|
obsolete ureteropelvic junction obstruction
|
MONDO_0029042 |
|
|
neurodevelopmental disorder with central and peripheral motor dysfunction
|
MONDO_0032698 |
|
|
hereditary thrombocytopenia with normal platelets
|
MONDO_0017057 |
|
|
leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome
|
MONDO_0030035 |
|
|
epilepsy, idiopathic generalized, susceptibility to, 15
|
MONDO_0032699 |
|
|
epilepsy, progressive myoclonic, 11
|
MONDO_0030034 |
|
|
neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures
|
MONDO_0030037 |
|
|
oocyte maturation defect 6
|
MONDO_0032696 |
|
|
neurodevelopmental disorder and language delay with or without structural brain abnormalities
|
MONDO_0032697 |
|
|
leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome
|
MONDO_0030036 |
|
|
intermittent maple syrup urine disease
|
MONDO_0017053 |
|
|
microcephaly 25, primary, autosomal recessive
|
MONDO_0032694 |
|
|
lissencephaly 10
|
MONDO_0030031 |
|
|
Nizon-Isidor syndrome
|
MONDO_0030030 |
|
|
thiamine-responsive maple syrup urine disease
|
MONDO_0017054 |
|
|
seizures, early-onset, with neurodegeneration and brain calcifications
|
MONDO_0030033 |
|
|
Galloway-Mowat syndrome 7
|
MONDO_0032692 |
|
|
mycophenolate mofetil embryopathy
|
MONDO_0017055 |
|
