|
isolated focal cortical dysplasia type Ic
|
MONDO_0017098 |
|
|
vertebral, cardiac, renal, and limb defects syndrome 3
|
MONDO_0030077 |
|
|
obsolete facioscapulohumeral dystrophy
|
MONDO_0017099 |
|
|
intellectual developmental disorder with ocular anomalies and distinctive facial features
|
MONDO_0859303 |
|
|
neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction
|
MONDO_0859304 |
|
|
unilateral focal polymicrogyria
|
MONDO_0017093 |
|
|
unilateral polymicrogyria
|
MONDO_0017092 |
|
|
isolated focal cortical dysplasia type Ia
|
MONDO_0017096 |
|
|
Neuronopathy, distal hereditary motor, type X
|
MONDO_0859300 |
|
|
neurodevelopmental disorder with language impairment and behavioral abnormalities
|
MONDO_0030060 |
|
|
arrhythmogenic right ventricular dysplasia, familial, 14
|
MONDO_0030062 |
|
|
periventricular nodular heterotopia 9
|
MONDO_0030061 |
|
|
Treacher Collins syndrome 4
|
MONDO_0030067 |
|
|
hyper-IgE recurrent infection syndrome 5, autosomal recessive
|
MONDO_0030069 |
|
|
episodic ataxia, type 9
|
MONDO_0030064 |
|
|
neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities
|
MONDO_0030063 |
|
|
granulomatous disease, chronic, autosomal recessive, 5
|
MONDO_0030066 |
|
|
agenesis of corpus callosum, cardiac, ocular, and genital syndrome
|
MONDO_0030065 |
|
|
diabetes mellitus, permanent neonatal 4
|
MONDO_0030089 |
|
|
diabetes mellitus, permanent neonatal 3
|
MONDO_0030088 |
|
