Category:Rare Diseases
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This is a category page. It lists all of the pages in category "Rare Diseases" as well as all subcategories of category "Rare Diseases" if any exist.
Pages in category "Rare Diseases"
The following 200 pages are in this category, out of 310 total.
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- Aaas
- ABCD syndrome
- Abdallat Davis Farrage syndrome
- Abruzzo Erickson syndrome
- Achiria
- Achondrogenesis
- Acquired generalized lipodystrophy
- Acral arteriolar ectasia
- Acrocephalosyndactyly
- Action Medical Research
- Acute interstitial pneumonitis
- Acytosiosis
- Adiposogenital dystrophy
- Aicardi syndrome
- AL amyloidosis
- Al-Raqad syndrome
- Alien hand syndrome
- Alpers syndrome
- Analbuminaemia
- Andermann syndrome
- Antisynthetase syndrome
- Aquagenic pruritus
- Arakawa's syndrome II
- Arrhinia
- Arterial tortuosity syndrome
- Ascher's syndrome
- Ataxia-pancytopenia syndrome
B
- Baller-Gerold syndrome
- Bardet-biedl syndrome
- Bare lymphocyte syndrome
- Barraquer-Simons syndrome
- Barraquer–Simons syndrome
- Barth
- Barth syndrome
- Benign symmetric lipomatosis
- Berdon syndrome
- Berk-Tabatznik syndrome
- Bhaskar Jagannathan syndrome
- Biemond syndrome
- Binder's syndrome
- Birt-Hogg-Dube syndrome
- Bonn
- Brachydactyly type A1
- Brachydactyly type C
- Buerger disease
- Burnside-Butler syndrome
C
- Carney syndrome
- Carnosinemia
- Cartilage hair hypoplasia
- Caudal duplication
- Centrifugal lipodystrophy
- Cerebrotendineous xanthomatosis
- Char syndrome
- Charge syndrome
- CHILD syndrome
- Chondrodysplasia, Grebe type
- Clinic for Special Children
- Cloverleaf skull
- CLOVES syndrome
- Cobb syndrome
- Cogan syndrome
- Cohen syndrome
- Congenital hypofibrinogenemia
- Copenhagen disease
- Cornelia de Lange syndrome
- Costello syndrome
- Cramp fasciculation syndrome
- Cryofibrinogenemia
- Currarino syndrome
- Currarino triad
- Cutis verticis gyrata
- Cyclic vomiting syndrome
D
E
F
- FACES syndrome
- Facial hemiatrophy
- Familial amyloid polyneuropathy
- Farber disease
- Femoral facial syndrome
- Fibrochondrogenesis
- Fibrodysplasia Ossificans Progressiva
- Fibrodysplasia ossificans progressiva
- Fibromuscular dysplasia
- Fibrosing mediastinitis
- Fibrous dysplasia
- Foerster's syndrome
- Fraser syndrome
G
H
- Hajdu-Cheney syndrome
- Hall
- Hallermann Streiff syndrome
- Hanhart syndrome
- Hardcastle syndrome
- Harding ataxia
- Harlequin-type ichthyosis
- Hemophilia b
- Hepatoerythropoietic porphyria
- Hercules
- Hereditary amyloidosis
- Heterotaxy syndrome
- Histiocytic sarcoma
- Hopkins syndrome
- Hunter
- Hydranencephaly
- Hypereosinophilic syndrome
- Hyperlysinemia
- Hypoprothrombinemia
I
K
L
- L1 syndrome
- Lachiewicz Sibley syndrome
- Laminopathy
- Large plaque parapsoriasis
- Lawrence
- Leena Peltonen-Palotie
- Leontiasis ossea
- Leri pleonosteosis
- Lesch Nyhan syndrome
- Leschke syndrome
- Lesch–Nyhan syndrome
- LIG4 syndrome
- Local gigantism
- Localized lichen myxedematosus
- Localized lipodystrophy
- Loeys-Dietz syndrome
- Lubinsky syndrome
- Lymphangiomyomatosis
- Lymphedema praecox
M
- Macleod
- Macrophagic myofasciitis
- Malignant triton tumor
- Malouf syndrome
- McLeod syndrome
- Mediastinal fibrosis
- Megaduodenum
- Meige disease
- Meige syndrome
- Melorheostosis
- Metachondromatosis
- Methaemalbuminaemia
- Mevalonate kinase deficiency
- Mickleson syndrome
- Microhydranencephaly
- Milo
- Mitchell
- Mobius syndrome
- Moebius syndrome
- Mondini dysplasia
- Mondor's disease
- Monostotic fibrous dysplasia
- Mortimer's disease
- Muckle
- Multifocal lymphangioendotheliomatosis
- Multiple sulfatase deficiency
- Myelokathexis
- Myositis ossificans