Leigh syndrome
ORPHA:506Lethal congenital contracture syndrome type 1
ORPHA:1486Lyme disease
ORPHA:91546Meige disease
ORPHA:90186Menkes disease
ORPHA:565Mucopolysaccharidosis type 7
ORPHA:584Naxos disease
ORPHA:34217Neuromyelitis optica spectrum disorder
ORPHA:71211Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies
ORPHA:592850Neuromyelitis optica spectrum disorder with anti-MOG antibodies
ORPHA:592856Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies
ORPHA:592869Neuronal ceroid lipofuscinosis
ORPHA:216Oculocerebrorenal syndrome of Lowe
ORPHA:534Osteochondritis dissecans
ORPHA:2764Panner disease
ORPHA:97336Parkinson-dementia complex of Guam
ORPHA:90020Peeling skin syndrome
ORPHA:817Peroxisomal disease
ORPHA:68373Persistent hyperplastic primary vitreous
ORPHA:91495Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome
ORPHA:363400Progressive familial intrahepatic cholestasis type 1
ORPHA:79306Psittacosis
ORPHA:660053Pyle disease
ORPHA:3005Salla disease
ORPHA:309334Sickle cell disease
ORPHA:275752Sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant
ORPHA:700085Sickle cell S-C disease
ORPHA:251365Sickle cell S-D Punjab disease
ORPHA:251370Sickle cell S-E disease
ORPHA:251375Steinert myotonic dystrophy
ORPHA:273Systemic-onset juvenile idiopathic arthritis
ORPHA:85414Transgrediens et progrediens palmoplantar keratoderma
ORPHA:495Tropical endomyocardial fibrosis
ORPHA:75565X-linked lymphoproliferative disease
ORPHA:2442