Rare Disease Library

Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.

Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"

74 matching diseasesClear search ×

Neuromyelitis optica spectrum disorder with anti-MOG antibodies

Devic disease · Devic syndrome

ORPHA:592856

Neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592869

Neuronal ceroid lipofuscinosis

NCL · NCL disease

ORPHA:216

Oculocerebrorenal syndrome of Lowe

Lowe disease · Lowe oculo-cerebro-renal syndrome

ORPHA:534

Ollier disease

Multiple Enchondromatosis type I · Enchondromatosis Spranger type I

ORPHA:296

Osteochondrosis of the metatarsal bone

Freiberg infraction · Avascular necrosis of the metatarsal bone

ORPHA:564003

Osteochondrosis of the tarsal bone

Avascular necrosis of the tarsal bone · Kohler disease

ORPHA:563991

Panner disease

Aseptic necrosis of the capital humerus · Osteochondrosis of the capital humerus

ORPHA:97336

Parkinson-dementia complex of Guam

Guam parkinsonism-dementia complex · Guam disease

ORPHA:90020

Progressive familial intrahepatic cholestasis type 1

Byler disease · FIC1 deficiency

ORPHA:79306

Proximal myotonic myopathy

Myotonic dystrophy type 2 · Proximal myotonic dystrophy

ORPHA:606

Pyle disease

SFRP4-related Pyle disease · Metaphyseal dysplasia, Pyle type

ORPHA:3005

Salla disease

ORPHA:309334

Sandhoff disease

ORPHA:796

Schilder disease

Myelinoclastic diffuse sclerosis

ORPHA:59298

Senior-Boichis syndrome

Boichis disease · Nephronophthisis-hepatic fibrosis syndrome

ORPHA:84081

Sickle cell disease

HbSS disease · SCD

ORPHA:275752

Sickle cell disease due to hemoglobin S and a non-S/non-C hemoglobin variant

HbSS disease · SCD

ORPHA:700085

Sickle cell S-C disease

Hemoglobin S-C disease · HbSC disease

ORPHA:251365

Sickle cell S-D Punjab disease

HbSD disease · Hemoglobin S-D Punjab disease

ORPHA:251370

Sickle cell S-E disease

HbSE disease · Hemoglobin S-E disease

ORPHA:251375

Steinert myotonic dystrophy

Myotonic dystrophy type 1 · Steinert disease

ORPHA:273

Systemic-onset juvenile idiopathic arthritis

Still disease · Systemic-onset JIA

ORPHA:85414

Tangier disease

ATP-binding cassette transporter A1 deficiency · Analphalipoproteinemia

ORPHA:31150

Transgrediens et progrediens palmoplantar keratoderma

Greither disease · Keratosis extremitatum hereditaria progrediens

ORPHA:495

Wagner disease

Dominant hyaloideoretinal dystrophy of Wagner · VCAN-related vitreoretinopathy

ORPHA:898