Category:Rare diseases
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 | Pages in this category should be moved to subcategories where applicable. This category may require frequent maintenance to avoid becoming too large. It should directly contain very few, if any, pages and should mainly contain subcategories. |
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A rare disease is technically defined as a disease that is found in fewer than 5 people per every 10,000 people.
Subcategories
This category has the following 17 subcategories, out of 17 total.
A
C
D
I
M
P
S
T
Pages in category "Rare diseases"
The following 200 pages are in this category, out of approximately 661 total. This list may not reflect recent changes (learn more).
(previous page) (next page)A
- Abdominal epilepsy
- Abetalipoproteinemia
- Absent adrenal gland
- Absent pulmonary valve syndrome
- Acheiropodia
- Achondroplasia
- Achromatopsia
- Acrodysostosis
- Acrofrontofacionasal dysostosis
- Acrogeria
- Acromesomelic dysplasia
- Acromicric dysplasia
- Acute eosinophilic pneumonia
- Adducted thumb syndrome
- Adenosine deaminase deficiency
- Adenosine monophosphate deaminase deficiency type 1
- Adenylosuccinate lyase deficiency
- Adermatoglyphia
- Adiposis dolorosa
- Adiposogenital dystrophy
- Adipsia
- Adrenoleukodystrophy
- Adult-onset Still's disease
- AIDS dysmorphic syndrome
- Albright's hereditary osteodystrophy
- Aldolase A deficiency
- Alexander disease
- Alopecia universalis
- ALOX12B
- Alpha-mannosidosis
- Alveolar capillary dysplasia
- Ameloblastic carcinoma
- Amyotrophic lateral sclerosis
- Anomalous aortic origin of a coronary artery
- Anorectal anomalies
- Antithrombin III deficiency
- Antley–Bixler syndrome
- Aortopulmonary septal defect
- Aphallia
- Aposthia
- Aquagenic urticaria
- Argininosuccinic aciduria
- Arrhinia
- Arthrogryposis
- Aspartylglucosaminuria
- Asplenia with cardiovascular anomalies
- Atelosteogenesis type I
- Atelosteogenesis, type II
- Athetoid cerebral palsy
- Atransferrinemia
- Atypical trigeminal neuralgia
- Autosomal dominant hypophosphatemic rickets
- Autosomal dominant polycystic kidney disease
- Autosomal dominant porencephaly type I
- Autosomal recessive polycystic kidney disease
B
- Balo concentric sclerosis
- Batten disease
- Behçet's disease
- Benign hereditary chorea
- Benign symmetric lipomatosis
- Beta-ketothiolase deficiency
- Beta-mannosidosis
- Bietti's crystalline dystrophy
- Biliary atresia
- Binswanger's disease
- Biotinidase deficiency
- Birdshot chorioretinopathy
- Bladder exstrophy
- Boomerang dysplasia
- Breast hypertrophy
C
- Camurati–Engelmann disease
- Canadian Organization for Rare Disorders
- Canavan disease
- Carcinosarcoma
- Carnitine palmitoyltransferase I deficiency
- Carnitine-acylcarnitine translocase deficiency
- Carnosinemia
- Caroli disease
- Catamenial pneumothorax
- Catecholaminergic polymorphic ventricular tachycardia
- CD55 deficiency
- Cenani–Lenz syndactylism
- Cerebroretinal microangiopathy with calcifications and cysts
- Cerebrotendineous xanthomatosis
- Cherubism
- Childhood granulomatous periorificial dermatitis
- Chondrolysis
- Chorea acanthocytosis
- Citrullinemia type I
- Cleidocranial dysostosis
- Cloacal exstrophy
- Clouston's hidrotic ectodermal dysplasia
- Cockayne syndrome
- Cole-Carpenter syndrome
- Colloid cyst
- Confluent and reticulated papillomatosis
- Congenital chloride diarrhea
- Congenital disorder of glycosylation type IIc
- Congenital ichthyosiform erythroderma
- Congenital insensitivity to pain
- Congenital insensitivity to pain with anhidrosis
- Congenital lactic acidosis
- Congenital stromal corneal dystrophy
- Conjoined twins
- Copenhagen disease
- Corticobasal degeneration
- Cranio-lenticulo-sutural dysplasia
- Craniodiaphyseal dysplasia
- Craniofrontonasal dysplasia
- Craniometaphyseal dysplasia
- Craniopagus parasiticus
- Creutzfeldt–Jakob disease
- Cruveilhier–Baumgarten disease
- Cutis laxa
- Cutis marmorata telangiectatica congenita
- Cyclic neutropenia
- Cystinosis
- Cytochrome b5 deficiency
- Cytochrome P450 oxidoreductase deficiency
D
- Danon disease
- Glut1 deficiency
- Deficiency of the interleukin-1–receptor antagonist
- Degos disease
- Dejerine–Sottas disease
- Dent's disease
- Denys–Drash syndrome
- Dermatopathia pigmentosa reticularis
- Dextrocardia
- Diabetes insipidus
- Diffuse panbronchiolitis
- Diphallia
- Dipygus
- List of disorders included in newborn screening programs
- Donohue syndrome
- Dracunculiasis
- Dupuytren's contracture
- Dysfibrinogenemia
- Dyskeratosis congenita
E
- EAST syndrome
- Ectopia cordis
- Ectrodactyly
- Enamel-renal syndrome
- Endocardial fibroelastosis
- Enterolith
- Epidermodysplasia verruciformis
- Epidermolysis bullosa
- Epidermolysis bullosa acquisita
- Epidermolysis bullosa simplex
- Epidermolytic hyperkeratosis
- Epispadias
- Epithelioid trophoblastic tumour
- Erdheim–Chester disease
- Erythrokeratodermia variabilis
- Erythromelalgia
- Erythropoietic protoporphyria
- Ewing's sarcoma
- Extramammary Paget's disease
F
- Fabry disease
- Facioscapulohumeral muscular dystrophy
- Familial atrial fibrillation
- Familial dysautonomia
- Familial hemiplegic migraine
- Familial isolated vitamin E deficiency
- Familial male-limited precocious puberty
- Farber disease
- Fatal insomnia
- Febrile neutrophilic dermatosis
- Fibrochondrogenesis
- Fibrodysplasia ossificans progressiva
- Fibromuscular dysplasia
- Fields' disease
- Finnish heritage disease
- Florid cutaneous papillomatosis
- Focal dermal hypoplasia
- Follicle-stimulating hormone insensitivity
- Friedreich's ataxia
- Frontonasal dysplasia
- Fucosidosis
- Fukuyama congenital muscular dystrophy
- Fumarase deficiency
G
- Galactocele
- Galactose epimerase deficiency
- Galactosialidosis
- Gangliosidosis
- Garre's sclerosing osteomyelitis
- Gastric atresia
- Gaucher's disease
- Genetic Alliance UK
- Gerodermia osteodysplastica
- Gestational trophoblastic disease
- Giant axonal neuropathy
- Giant platelet disorder
- Giant-cell tumor of the tendon sheath
- Glanzmann's thrombasthenia
- Glassy cell carcinoma of the cervix
- Glucagonoma
- Glucose-galactose malabsorption
