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"

94 matching diseasesClear search ×

Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome

HbSS disease · HPFH-sickle cell disease syndrome

ORPHA:251380

Histoplasmosis

Darling disease

ORPHA:390

HSD10 disease

2-methyl-3-hydroxybutyric aciduria · 2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency

ORPHA:391417

Hypopigmentation-punctate palmoplantar keratoderma syndrome

Cole disease · Guttate hypopigmentation and punctate palmoplantar keratoderma

ORPHA:324561

Infantile mercury poisoning

Erythroedema polyneuritis · Feer disease

ORPHA:247165

Invasive non-typhoidal salmonellosis

Invasive non-typhoidal salmonella disease · iNTS disease

ORPHA:324648

Lafora disease

EPM2 · PME type 2

ORPHA:501

Leber plus disease

LHON plus disease

ORPHA:99718

Ledderhose disease

Plantar fibromatosis

ORPHA:199251

Leigh syndrome

Infantile subacute necrotizing encephalopathy · Leigh disease

ORPHA:506

Lethal congenital contracture syndrome type 1

Herva disease · LCCS1

ORPHA:1486

Lyme disease

Lyme borreliosis

ORPHA:91546

Lysosomal disease

ORPHA:68366

Meige disease

Hereditary lymphedema type II · Meige lymphedema

ORPHA:90186

Mucopolysaccharidosis type 7

Beta-glucuronidase deficiency · MPS7

ORPHA:584

Multiple symmetric lipomatosis

Cephalothoracic lipodystrophy · Familial benign cervical lipomatosis

ORPHA:2398

Naxos disease

KWWH type I · Keratoderma with woolly hair type I

ORPHA:34217

Neuromyelitis optica spectrum disorder

Devic disease · Devic syndrome

ORPHA:71211

Neuromyelitis optica spectrum disorder with anti-AQP4 antibodies

Devic disease · Devic syndrome

ORPHA:592850

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

Non-amyloid monoclonal immunoglobulin deposition disease

Non-amyloid MIDD · Randall disease

ORPHA:86861

Oculocerebrorenal syndrome of Lowe

Lowe disease · Lowe oculo-cerebro-renal syndrome

ORPHA:534

Osteochondritis dissecans

König disease

ORPHA:2764

Osteogenesis imperfecta

Brittle bone disease · Glass bone disease

ORPHA:666

Parkinson-dementia complex of Guam

Guam parkinsonism-dementia complex · Guam disease

ORPHA:90020

Peeling skin syndrome

Deciduous skin · Familial continuous skin peeling syndrome

ORPHA:817

Persistent hyperplastic primary vitreous

Non-syndromic congenital retinal non-attachment · PFVS

ORPHA:91495

Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome

Severe neurodegenerative syndrome due to BSCL2 deficiency · Celia encephalopathy

ORPHA:363400

Progressive familial intrahepatic cholestasis type 1

Byler disease · FIC1 deficiency

ORPHA:79306

Pyle disease

SFRP4-related Pyle disease · Metaphyseal dysplasia, Pyle type

ORPHA:3005

Rare lens disease

ORPHA:98639

Salla disease

ORPHA:309334

Sandhoff disease

ORPHA:796

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

Sinding-Larsen-Johansson disease

Aseptic necrosis of patella · Osteochondrosis of patella

ORPHA:97337

Systemic-onset juvenile idiopathic arthritis

Still disease · Systemic-onset JIA

ORPHA:85414

Tropical endomyocardial fibrosis

Davies disease · TEMF

ORPHA:75565

Upington disease

Hip dysplasia-enchondromata-ecchondroma syndrome

ORPHA:3408

Von Hippel-Lindau disease

Familial cerebelloretinal angiomatosis · Lindau disease

ORPHA:892

X-linked lymphoproliferative disease

Duncan disease · Purtilo syndrome

ORPHA:2442