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"

93 matching diseasesClear search ×

IgG4-related dacryoadenitis and sialadenitis

Chronic dacryoadenitis and sialadenitis · Mikulicz disease

ORPHA:79078

Infantile mercury poisoning

Erythroedema polyneuritis · Feer disease

ORPHA:247165

Invasive non-typhoidal salmonellosis

Invasive non-typhoidal salmonella disease · iNTS disease

ORPHA:324648

Kyasanur forest disease

Kyasanur hemorrhagic fever · Monkey disease

ORPHA:319254

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

Mal de Meleda

Meleda disease

ORPHA:87503

Medullar disease

ORPHA:102000

Meige disease

Hereditary lymphedema type II · Meige lymphedema

ORPHA:90186

Ménétrier disease

Hypoproteinemic hypertrophic gastropathy · Giant hypertrophic gastritis

ORPHA:2494

Menkes disease

Menkes kinky hair disease · MD

ORPHA:565

Methionine adenosyltransferase I/III deficiency

MAT I/III deficiency · Mudd's disease

ORPHA:168598

Milroy disease

Hereditary lymphedema type I · Nonne-Milroy lymphedema

ORPHA:79452

Moyamoya disease

Idiopathic Moyamoya disease

ORPHA:2573

Mucopolysaccharidosis type 4

MPS4 · MPSIV

ORPHA:582

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

Occult macular dystrophy

OCMD · OMD

ORPHA:247834

Oculocerebrorenal syndrome of Lowe

Lowe disease · Lowe oculo-cerebro-renal syndrome

ORPHA:534

Osteochondritis dissecans

König disease

ORPHA:2764

Osteopetrosis with renal tubular acidosis

Carbonic anhydrase 2 deficiency · Guibaud-Vainsel syndrome

ORPHA:2785

Parkinson-dementia complex of Guam

Guam parkinsonism-dementia complex · Guam disease

ORPHA:90020

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 cardiac disease

ORPHA:97929

Salla disease

ORPHA:309334

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

Stargardt disease

Fundus flavimaculatus · Stargardt 1

ORPHA:827

Systemic-onset juvenile idiopathic arthritis

Still disease · Systemic-onset JIA

ORPHA:85414

Tropical endomyocardial fibrosis

Davies disease · TEMF

ORPHA:75565

Whipple disease

Intestinal lipodystrophy

ORPHA:3452

X-linked lymphoproliferative disease

Duncan disease · Purtilo syndrome

ORPHA:2442