All terms in MONDO
| Label |
Id |
Description |
|
immunodeficiency 80 with or without congenital cardiomyopathy
|
MONDO_0030266 |
|
|
Brunet-Wagner neurodevelopmental syndrome
|
MONDO_0859217 |
|
|
developmental delay with variable neurologic and brain abnormalities
|
MONDO_0859218 |
|
|
developmental and epileptic encephalopathy 6B
|
MONDO_0030268 |
|
|
Rauch-Steindl syndrome
|
MONDO_0859219 |
|
|
pontocerebellar hypoplasia, type 1F
|
MONDO_0030261 |
|
|
Marbach-Schaaf neurodevelopmental syndrome
|
MONDO_0859214 |
|
|
dystonia, early-onset, and/or spastic paraplegia
|
MONDO_0859215 |
|
|
leukodystrophy, hypomyelinating, 21
|
MONDO_0030263 |
|
|
neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis
|
MONDO_0859216 |
|
|
chromosome 16q12 duplication syndrome
|
MONDO_0859210 |
|
|
neurodevelopmental disorder with hyperkinetic movements and dyskinesia
|
MONDO_0859211 |
|
|
neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus
|
MONDO_0859212 |
|
|
pontocerebellar hypoplasia, type 15
|
MONDO_0030259 |
|
|
pontocerebellar hypoplasia, type 14
|
MONDO_0030258 |
|
|
angioedema, hereditary, 5
|
MONDO_0030293 |
|
|
neurodevelopmental disorder with hearing loss and spasticity
|
MONDO_0859206 |
|
|
angioedema, hereditary, 8
|
MONDO_0030298 |
|
|
neurodevelopmental disorder with hypotonia and gross motor and speech delay
|
MONDO_0859207 |
|
|
Hengel-Maroofian-Schols syndrome
|
MONDO_0859208 |
|
