Genetics

Myotonic dystrophy

TGM3 gene

Unverricht-Lundborg disease

Atelosteogenesis type 2

Hepatic veno-occlusive disease with immunodeficiency

Narcolepsy

CLCN2-related leukoencephalopathy

Miyoshi myopathy

NEB gene

Ovarian cancer

FAH gene

Biotinidase deficiency