Invasive non-typhoidal salmonellosis
ORPHA:324648Leigh syndrome
ORPHA:506Lethal congenital contracture syndrome type 1
ORPHA:1486Lyme disease
ORPHA:91546Meige disease
ORPHA:90186Mucopolysaccharidosis 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:216Non-amyloid monoclonal immunoglobulin deposition disease
ORPHA:86861Oculocerebrorenal syndrome of Lowe
ORPHA:534Osteochondritis dissecans
ORPHA:2764Parkinson-dementia complex of Guam
ORPHA:90020Perinatal lethal hypophosphatasia
ORPHA:247623Persistent hyperplastic primary vitreous
ORPHA:91495Prenatal benign hypophosphatasia
ORPHA:247638Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome
ORPHA:363400Progressive familial intrahepatic cholestasis type 1
ORPHA:79306Proximal myotonic myopathy
ORPHA:606Pyle disease
ORPHA:3005Rare adrenal disease
ORPHA:101954Rare allergic disease
ORPHA:98050Rare bone disease
ORPHA:93419Rare cardiac disease
ORPHA:97929Rare genetic disease
ORPHA:98053Rare hepatic disease
ORPHA:57146Rare immune disease
ORPHA:98004Rare lens disease
ORPHA:98639Rare neoplastic disease
ORPHA:250908Rare renal disease
ORPHA:93626Rare respiratory disease
ORPHA:97955Rare skin disease
ORPHA:89826Rare systemic disease
ORPHA:182222Rare teratologic disease
ORPHA:52662Rare thyroid disease
ORPHA:101955Rare vascular disease
ORPHA:68362Rare viral disease
ORPHA:163585Salla 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:251375Systemic-onset juvenile idiopathic arthritis
ORPHA:85414Tropical endomyocardial fibrosis
ORPHA:75565