PUM1-related cerebellar ataxia
ORPHA:642747Adult-onset Steinert myotonic dystrophy
ORPHA:589830Adult-onset Still disease
ORPHA:829Carnitine palmitoyl transferase II deficiency, myopathic form
ORPHA:228302Ocular cystinosis
ORPHA:411641Overlap myositis
ORPHA:206572Primary lateral sclerosis
ORPHA:35689Young adult-onset distal hereditary motor neuropathy
ORPHA:314485