Category:Rare diseases
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Template:Sister project Template:Category diffuse Template:Cat main A rare disease is technically defined (in the European Union) as a disease that is found in fewer than 5 people per every 10,000 people. Template:CatAutoTOC
Template:AnchorPages in category "Rare diseases"
The following 146 pages are in this category, out of 146 total.
A
- Abetalipoproteinemia
- Acheiropodia
- Achondroplasia
- Achromatopsia
- Acute disseminated encephalomyelitis
- Adducted thumb syndrome
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency type 1
- Adrenoleukodystrophy
- Alexander disease
- Alkaptonuria
- Alopecia universalis
- Alpha-mannosidosis
- Anorectal anomalies
- Arthrogryposis
- Autosomal dominant polycystic kidney disease
B
C
- Canavan disease
- Caroli disease
- Castleman disease
- Cenani–Lenz syndactylism
- Chorea-acanthocytosis
- Cloacal exstrophy
- Congenital hyperinsulinism
- Congenital insensitivity to pain
- Congenital insensitivity to pain with anhidrosis
- Conjoined twins
- Craniodiaphyseal dysplasia
- Craniopagus parasiticus
- Creutzfeldt–Jakob disease
- Cystic fibrosis
D
E
G
H
- Haemophilia
- Hallermann–Streiff syndrome
- Harlequin-type ichthyosis
- Hereditary fructose intolerance
- Hereditary multiple exostoses
- Hereditary spastic paraplegia
- Hidradenitis suppurativa
- Hirschsprung's disease
- Hydranencephaly
- Hyperacusis
- Hyperkalemic periodic paralysis
- Hypertrichosis
- Hypoparathyroidism
- Hypopituitarism
I
L
M
N
P
- Parasitic twin
- Paroxysmal nocturnal hemoglobinuria
- Pelizaeus–Merzbacher disease
- Pelvic lipomatosis
- Phenylketonuria
- Plummer–Vinson syndrome
- Polyorchidism
- Porphyria cutanea tarda
- Pre-eclampsia
- Primary ciliary dyskinesia
- Progeria
- Progressive multifocal leukoencephalopathy
- Progressive supranuclear palsy
- Propionic acidemia
- Pulmonary alveolar proteinosis
- Pulmonary hypertension