Category
page 1Neurogenetic disorders
Asperger syndrome
neurodevelopmental disorder; type of autism
Tourette syndrome
neurodevelopmental condition
fragile X syndrome
congenital disorder of nervous system
McLeod syndrome
rare disease
encephalopathy due to GLUT1 deficiency
disease
Dejerine–Sottas disease
a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting
dentatorubral-pallidoluysian atrophy
congenital disorder of nervous system
Allan-Herndon-Dudley syndrome
congenital disorder of nervous system
Kohlschütter-Tönz syndrome
rare inherited human disease
hereditary sensory and autonomic neuropathy
congenital disorder of nervous system
hereditary motor and sensory neuropathy
congenital disorder of nervous system
biotin-responsive basal ganglia disease
Human disease
non-syndromic pontocerebellar hypoplasia
Human disease