Neurogenetics
- Aicardi-Goutières syndrome
- Alternating hemiplegia of childhood 2 (AHC2)
- CADASIL
- Dentatorubral pallidoluysian atrophy (DRPLA)
- Episodic ataxia
- Cerebral Haemorrhage, hereditary (HCHWA-D)
- Huntington's disease (HD)
- Huntington's disease-like 2 (HDL2)
- Hyperekplexia (familial Startle disease)
- Neuronal ceroid lipofuscinosis (NCL)
- Migraine, familial hemiplegic (FHM)
- Myoclonic dystonia
- Retinal vasculopathy with cerebral leukodystrophy (RVCL)