Lethal congenital contracture syndrome type 1
ORPHA:1486Lyme disease
ORPHA:91546Mal de Meleda
ORPHA:87503Meige disease
ORPHA:90186Menkes disease
ORPHA:565Methionine adenosyltransferase I/III deficiency
ORPHA:168598Milroy disease
ORPHA:79452Mitochondrial oxidative phosphorylation disorder
ORPHA:223713Moyamoya disease
ORPHA:2573Mucolipidosis type II
ORPHA:576Mucopolysaccharidosis type 4
ORPHA:582Mucopolysaccharidosis type 7
ORPHA:584Multiple myeloma
ORPHA:29073Multiple sulfatase deficiency
ORPHA:585Nasu-Hakola disease
ORPHA:2770Naxos 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:216Nipah virus disease
ORPHA:99825Non-amyloid monoclonal immunoglobulin deposition disease
ORPHA:86861Norrie disease
ORPHA:649Occult macular dystrophy
ORPHA:247834Oculocerebrorenal syndrome of Lowe
ORPHA:534Oguchi disease
ORPHA:75382Ollier disease
ORPHA:296Osteochondritis dissecans
ORPHA:2764Osteochondrosis of the tarsal bone
ORPHA:563991Panner disease
ORPHA:97336Parkinson-dementia complex of Guam
ORPHA:90020Persistent hyperplastic primary vitreous
ORPHA:91495Polycythemia vera
ORPHA:729Pontocerebellar hypoplasia type 1
ORPHA:2254Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome
ORPHA:363400Progressive familial intrahepatic cholestasis type 1
ORPHA:79306Proximal myotonic myopathy
ORPHA:606Psittacosis
ORPHA:660053Pyle disease
ORPHA:3005Reticular dysgenesis
ORPHA:33355Salla disease
ORPHA:309334Senior-Boichis syndrome
ORPHA:84081Sickle 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:251375