OBSOLETE: Adult neuronal ceroid lipofuscinosis
ORPHA:79262Adult CLN1 disease
ORPHA:699745Adult CLN5 disease
ORPHA:699812Adult CLN6 disease
ORPHA:700477Adult hypophosphatasia
ORPHA:247676Adult Krabbe disease
ORPHA:206448Adult Refsum disease
ORPHA:773Adult-onset Steinert myotonic dystrophy
ORPHA:589830Adult-onset Still disease
ORPHA:829Neuronal ceroid lipofuscinosis
ORPHA:216OBSOLETE: Adult chronic recurrent multifocal osteomyelitis
ORPHA:93668OBSOLETE: Argyrophilic grain disease
ORPHA:97342OBSOLETE: Autosomal dominant Opitz G/BBB syndrome
ORPHA:306588OBSOLETE: Basement membrane disease
ORPHA:93550OBSOLETE: Binswanger disease
ORPHA:1249OBSOLETE: Cardiac disease with cataract
ORPHA:98647OBSOLETE: CLN4A disease
ORPHA:228340OBSOLETE: CLN9 disease
ORPHA:228357OBSOLETE: Farmer's lung disease
ORPHA:99906OBSOLETE: Glycogen storage disease due to acid maltase deficiency, adult onset
ORPHA:308604OBSOLETE: Glycogen storage disease due to acid maltase deficiency, juvenile onset
ORPHA:308573OBSOLETE: Hemochromatosis type 4
ORPHA:139491OBSOLETE: Infantile neuronal ceroid lipofuscinosis
ORPHA:79263OBSOLETE: Juvenile neuronal ceroid lipofuscinosis
ORPHA:79264OBSOLETE: Late infantile neuronal ceroid lipofuscinosis
ORPHA:168491OBSOLETE: Letterer-Siwe disease
ORPHA:99870OBSOLETE: Multicentric Castleman disease
ORPHA:93686OBSOLETE: Niemann-Pick disease type E
ORPHA:99022OBSOLETE: Pediatric Castleman disease
ORPHA:93682OBSOLETE: Pigeon-breeder lung disease
ORPHA:99908OBSOLETE: Primary glomerular disease
ORPHA:102373OBSOLETE: Rare acquired eye disease
ORPHA:101949OBSOLETE: Secondary glomerular disease
ORPHA:93551OBSOLETE: Sporadic Leigh syndrome
ORPHA:255199OBSOLETE: Tay-Sachs disease, B1 variant
ORPHA:309239OBSOLETE: Unstable hemoglobin disease
ORPHA:99139