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general/rare-diseases

Surf Wiki
Rare disease

Disease affecting a small percentage of the population

general/rare-diseases
Ectrodactyly

Malformation of the central digit(s) of the hand or foot

general/rare-diseases
Dercum's disease

Medical condition

general/rare-diseases
Cranio-lenticulo-sutural dysplasia
general/rare-diseases
Degos disease
general/rare-diseases
Ectopia cordis

Birth defect in which the heart is positioned outside the thorax

general/rare-diseases
Finnish heritage disease

Group of autosomal recessive genetic disorders that affect Finns much more frequently

general/rare-diseases
Birdshot chorioretinopathy
general/rare-diseases
Erdheim–Chester disease
general/rare-diseases
Asplenia with cardiovascular anomalies
general/rare-diseases
Giant platelet disorder
general/rare-diseases
GM1 gangliosidoses
general/rare-diseases
Iridogoniodysgenesis, dominant type
general/rare-diseases
Harlequin syndrome
general/rare-diseases
Idiopathic CD4+ lymphocytopenia
general/rare-diseases
Lysosomal acid lipase deficiency
general/rare-diseases
Lethal congenital contracture syndrome
general/rare-diseases
Infantile free sialic acid storage disease
general/rare-diseases
Laryngeal papillomatosis
general/rare-diseases
Neuromyotonia
general/rare-diseases
Letterer–Siwe disease
general/rare-diseases
Plantar fibromatosis

Thickening of the feet's deep connective tissue (fascia)

general/rare-diseases
WHIM syndrome
general/rare-diseases
Waldmann disease
general/rare-diseases
Synovial chondromatosis
general/rare-diseases
Urticaria pigmentosa

Most common form of cutaneous mastocytosis

general/rare-diseases
Short-chain acyl-coenzyme A dehydrogenase deficiency
general/rare-diseases
Rombo syndrome
general/rare-diseases
Oculodentodigital dysplasia
general/rare-diseases
Smith–Fineman–Myers syndrome
general/rare-diseases
Reticular dysgenesis
general/rare-diseases
Urofacial syndrome
general/rare-diseases
Chorea-acanthocytosis

Rare autosomal recessive genetic condition

general/rare-diseases
Multiple epiphyseal dysplasia

Rare genetic disorder

general/rare-diseases
Florid cutaneous papillomatosis
general/rare-diseases
Paroxysmal nocturnal hemoglobinuria

Blood disease in which red blood cells are attacked by the immune system

general/rare-diseases
Fucosidosis
general/rare-diseases
Enterolith

Solid mineral mass formed in the gastrointestinal system

general/rare-diseases
Non-24-hour sleep–wake disorder

Medical condition

general/rare-diseases
Farber disease
general/rare-diseases
Alveolar capillary dysplasia

Rare lung disease, present at birth and treatable by lung transplants

general/rare-diseases
Becker muscular dystrophy

Genetic muscle disorder

general/rare-diseases
Lethal arthrogryposis with anterior horn cell disease
general/rare-diseases
Acromicric dysplasia
general/rare-diseases
Lymphomatoid papulosis
general/rare-diseases
Ribose-5-phosphate isomerase deficiency

Rare metabolic genetic disorder resulting in leukoencephalopathy

general/rare-diseases