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neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures

Disease Summary
Associated Targets (1)
Tbio

1


Uniprot Description An autosomal recessive disorder characterized by profound developmental delay, progressive spastic quadriplegia and contractures, early-onset refractory epilepsy in most patients, and brain malformations. Neuroimaging shows ventriculomegaly, reduced cerebral white matter volume, and thinning of cerebral gray matter.
Mondo Term and Equivalent IDs
MONDO:0060704:  neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures
UMLS:CN244929: