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"

73 matching diseasesClear search ×

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

Juvenile amyotrophic lateral sclerosis

ALS · Charcot disease

ORPHA:300605

Keratoderma hereditarium mutilans with ichthyosis

Camisa disease · Keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome

ORPHA:79395

Lyme disease

Lyme borreliosis

ORPHA:91546

Medullar disease

ORPHA:102000

Mucolipidosis type II

I-cell disease · N-acetylglucosamine 1-phosphotransferase deficiency

ORPHA:576

Mucopolysaccharidosis type 7

Beta-glucuronidase deficiency · MPS7

ORPHA:584

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

Oculocerebrorenal syndrome of Lowe

Lowe disease · Lowe oculo-cerebro-renal syndrome

ORPHA:534

Parkinson-dementia complex of Guam

Guam parkinsonism-dementia complex · Guam disease

ORPHA:90020

Progressive encephalopathy-severe neurodegeneration-lipodystrophy syndrome

Severe neurodegenerative syndrome due to BSCL2 deficiency · Celia encephalopathy

ORPHA:363400

Pyle disease

SFRP4-related Pyle disease · Metaphyseal dysplasia, Pyle type

ORPHA:3005

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

Upington disease

Hip dysplasia-enchondromata-ecchondroma syndrome

ORPHA:3408

Wilson disease

Hepatolenticular degeneration

ORPHA:905