Hypopigmentation-punctate palmoplantar keratoderma syndrome
ORPHA:324561Infantile mercury poisoning
ORPHA:247165Invasive non-typhoidal salmonellosis
ORPHA:324648Juvenile amyotrophic lateral sclerosis
ORPHA:300605Keratoderma hereditarium mutilans with ichthyosis
ORPHA:79395Lyme disease
ORPHA:91546Medullar disease
ORPHA:102000Mucolipidosis type II
ORPHA:576Mucopolysaccharidosis type 7
ORPHA:584Neuromyelitis 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:534Parkinson-dementia complex of Guam
ORPHA:90020Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome
ORPHA:363400Pyle disease
ORPHA:3005Sickle 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:251375Upington disease
ORPHA:3408Wilson disease
ORPHA:905