Category:Rare diseases
From HandWiki
Here is a list of articles in the Rare diseases category of the Medicine portal.
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. |
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.
Subcategories
This category has the following 5 subcategories, out of 5 total.
C
- Rare cancers (124 P)
- Cystic fibrosis (27 P)
I
- Rare infectious diseases (39 P)
M
- Motor neuron diseases (27 P)
S
- Rare syndromes (414 P)
Pages in category "Rare diseases"
The following 200 pages are in this category, out of 804 total.
(previous page) (next page)F
- Medicine:Fields' disease
- Medicine:Filippi Syndrome
- Medicine:Filippi syndrome
- Biology:Finnish heritage disease
- Medicine:Florid cutaneous papillomatosis
- Medicine:Focal dermal hypoplasia
- Biology:Follicle-stimulating hormone insensitivity
- Medicine:Friedreich's ataxia
- Medicine:Frontonasal dysplasia
- Medicine:Fucosidosis
- Medicine:Fukuyama congenital muscular dystrophy
- Medicine:Fumarase deficiency
G
- Medicine:Galactocele
- Medicine:Galactose epimerase deficiency
- Medicine:Galactosialidosis
- Medicine:Gangliosidosis
- Medicine:Garre's sclerosing osteomyelitis
- Medicine:Gastric atresia
- Medicine:Gaucher's disease
- Organization:Genetic Alliance UK
- Medicine:Genu recurvatum
- Medicine:Gerodermia osteodysplastica
- Medicine:Gestational trophoblastic disease
- Medicine:Giant axonal neuropathy
- Medicine:Giant platelet disorder
- Medicine:Giant-cell tumor of the tendon sheath
- Biography:Gigantism
- Medicine:Glanzmann's thrombasthenia
- Medicine:Glassy cell carcinoma of the cervix
- Medicine:Glucose-galactose malabsorption
- Medicine:Glutaric acidemia type 2
- Medicine:Glutaric aciduria type 1
- Medicine:Glutathione synthetase deficiency
- Medicine:Glycine encephalopathy
- Medicine:Glycogen storage disease
- Medicine:Glycogen storage disease type II
- Medicine:Glycogen storage disease type VI
- Medicine:GM1 gangliosidoses
- Medicine:GM2 gangliosidoses
- Medicine:GM2-gangliosidosis, AB variant
- Medicine:Gonadal dysgenesis
- Medicine:Gonadotropin insensitivity
- Medicine:Gonadotropin-releasing hormone insensitivity
- Medicine:Gorham's disease
- Medicine:GOSR2-related progressive myoclonus ataxia
- Medicine:Granuloma annulare
- Medicine:Granulomatosis with polyangiitis
- Medicine:Guanidinoacetate methyltransferase deficiency
- Medicine:Guizar–Vasquez–Sanchez–Manzano syndrome
- Medicine:Gunther disease
H
- Medicine:Haemolacria
- Medicine:Hailey–Hailey disease
- Medicine:Hallermann–Streiff syndrome
- Medicine:Halo nevus
- Medicine:Halperin-Birk syndrome
- Medicine:Chronic multifocal Langerhans cell histiocytosis
- Medicine:Harlequin syndrome
- Medicine:Harlequin-type ichthyosis
- Medicine:Hartnup disease
- Medicine:Hemiballismus
- Medicine:Hemifacial hypertrophy
- Medicine:Hemihydranencephaly
- Medicine:Hemimegalencephaly
- Medicine:Hemiplegic migraine
- Medicine:Hemoglobinemia
- Medicine:Hepatic veno-occlusive disease
- Medicine:Hereditary fructose intolerance
- Medicine:Hereditary leiomyomatosis and renal cell cancer syndrome
- Medicine:Hereditary leiomyomatosis and renal cell carcinoma
- Medicine:Hereditary mucoepithelial dysplasia
- Medicine:Hereditary multiple exostoses
- Medicine:Hereditary neuralgic amyotrophy
- Medicine:Hereditary sensory and autonomic neuropathy
- Medicine:Hereditary sensory and autonomic neuropathy type I
- Medicine:Hereditary spastic paraplegia
- Medicine:Hidradenitis suppurativa
- Medicine:Hirschsprung's disease
- Medicine:Histidinemia
- Medicine:HNRNPH2-related disorders
- Medicine:Holocarboxylase synthetase deficiency
- Medicine:Hyaluronidase deficiency
- Medicine:Hydranencephaly
- Medicine:Hyperacusis
- Medicine:Hyperekplexia
- Medicine:Hyperkalemic periodic paralysis
- Medicine:Hyperlysinemia
- Medicine:Hyperprolinemia
- Medicine:Hypertrichosis
- Medicine:Hypertryptophanemia
- Medicine:Hypervalinemia
- Medicine:Hypocementosis
- Medicine:Hypochondroplasia
- Medicine:Hypodysfibrinogenemia
- Medicine:Hypohidrotic ectodermal dysplasia
- Medicine:Hypokalemic periodic paralysis
- Medicine:Hypoparathyroidism
- Medicine:Hypophosphatasia
- Medicine:Hypopituitarism
- Medicine:Hypoplastic left heart syndrome
- Biology:Hypotransferrinemia
- Medicine:Hypotrichosis with juvenile macular dystrophy
I
- Medicine:I-cell disease
- Medicine:ICD coding for rare diseases
- Medicine:Ichthyosis
- Medicine:Ichthyosis bullosa of Siemens
- Medicine:Ichthyosis follicularis with alopecia and photophobia syndrome
- Medicine:Ichthyosis hystrix
- Medicine:Ichthyosis vulgaris
- Medicine:Idiopathic CD4+ lymphocytopenia
- Medicine:Idiopathic granulomatous hepatitis
- Medicine:Idiopathic sclerosing mesenteritis
- Medicine:Immune thrombocytopenic purpura
- Medicine:Iminoglycinuria
- Medicine:Impossible syndrome
- Medicine:Inborn errors of steroid metabolism
- Medicine:Incontinentia pigmenti
- Medicine:Indium lung
- Medicine:Infantile digital fibromatosis
- Medicine:Infantile free sialic acid storage disease
- Medicine:Infantile myofibromatosis
- Medicine:Infantile neuroaxonal dystrophy
- Medicine:Infantile Refsum disease
- Medicine:Iniencephaly
- Medicine:Intellectual disability-spasticity-ectrodactyly syndrome
- Medicine:Intestinal atresia
- Medicine:Iridogoniodysgenesis, dominant type
- Medicine:Iris hypoplasia with glaucoma
- Medicine:Ischiopatellar dysplasia
- Medicine:Isolated 17,20-lyase deficiency
- Medicine:Isovaleric acidemia
J
K
- Medicine:Spinal and bulbar muscular atrophy
- Medicine:Keratolytic winter erythema
- Medicine:Keratomalacia
- Medicine:Kernicterus
- Medicine:Kienböck's disease
- Medicine:Kikuchi disease
- Medicine:Kimura's disease
- Medicine:Kleeblattschaedel
- Medicine:Kleeblattschaedel syndrome
- Medicine:Kniest dysplasia
- Medicine:Köhler disease
- Medicine:Kosaki overgrowth syndrome
- Medicine:Krabbe disease
- Medicine:Kufs disease
L
- Medicine:Lafora disease
- Medicine:Lamb-Shaffer syndrome
- Medicine:Lamellar ichthyosis
- Medicine:Langerhans cell histiocytosis
- Medicine:Laryngeal papillomatosis
- Medicine:Laurence–Moon syndrome
- Medicine:Leber congenital amaurosis
- Medicine:Leber's congenital amaurosis
- Medicine:Legg–Calvé–Perthes disease
- Medicine:Leontiasis ossea
- Medicine:Léri–Weill dyschondrosteosis
- Medicine:Lethal arthrogryposis with anterior horn cell disease
- Medicine:Lethal congenital contracture syndrome
- Medicine:Letterer–Siwe disease
- Medicine:Leukocyte adhesion deficiency
- Medicine:Leukocyte adhesion deficiency-1
- Medicine:Leukodystrophy
- Medicine:Leukoencephalopathy with vanishing white matter
- Medicine:Leydig cell hypoplasia
- Medicine:Lhermitte–Duclos disease
- Medicine:Li–Fraumeni syndrome
- Medicine:Limb body wall complex
- Medicine:Lipofibromatosis
- Medicine:Lipoid congenital adrenal hyperplasia
- Medicine:Lipoprotein lipase deficiency
- Medicine:Lipschütz ulcer
- Biology:Ljungan virus
- Medicine:Loeys–Dietz syndrome
- Medicine:LPS-responsive beige-like anchor protein deficiency
- Medicine:Lutembacher's syndrome
- Medicine:Lymphangioleiomyomatosis
- Medicine:Lymphangiomatosis
- Medicine:Lymphatic malformation 6 syndrome
- Medicine:Lymphomatoid papulosis
- Medicine:Lysinuric protein intolerance
- Medicine:Lysosomal acid lipase deficiency
M
- Medicine:Machado–Joseph disease
- Medicine:Macrocephaly-capillary malformation
- Unsolved:Macrophagic myofasciitis
- Medicine:Macular hypoplasia
- Medicine:Malakoplakia
- Medicine:Malignant hyperthermia
- Medicine:Malignant infantile osteopetrosis
- Medicine:Malonyl-CoA decarboxylase deficiency
- Medicine:Mandibulofacial dysostosis-microcephaly syndrome
- Medicine:Maple syrup urine disease
- Medicine:Mastocytosis
- Medicine:May–Hegglin anomaly