rare-diseases
Articles
- Erdheim–Chester disease
- Neuromyotonia
- Degos disease
- Lethal arthrogryposis with anterior horn cell disease
- Reticular dysgenesis
- Synovial chondromatosis
- Alveolar capillary dysplasiaRare lung disease, present at birth and treatable by lung transplants
- Smith–Fineman–Myers syndrome
- Neuromyotonia
- Erdheim–Chester disease
- Lymphomatoid papulosis
- Oculodentodigital dysplasia
- Letterer–Siwe disease
- Lymphomatoid papulosis
- Oculodentodigital dysplasia
- Letterer–Siwe disease
- Non-24-hour sleep–wake disorderMedical condition
- Becker muscular dystrophyGenetic muscle disorder
- Lymphomatoid papulosis
- Oculodentodigital dysplasia
- Letterer–Siwe disease
- Rare diseaseDisease affecting a small percentage of the population
- Birdshot chorioretinopathy
- Multiple epiphyseal dysplasiaRare genetic disorder
- Paroxysmal nocturnal hemoglobinuriaBlood disease in which red blood cells are attacked by the immune system
- Chorea-acanthocytosisRare autosomal recessive genetic condition
- Paroxysmal nocturnal hemoglobinuriaBlood disease in which red blood cells are attacked by the immune system
- Short-chain acyl-coenzyme A dehydrogenase deficiency
- Cranio-lenticulo-sutural dysplasia
- Acromicric dysplasia
- Synovial chondromatosis
- Alveolar capillary dysplasiaRare lung disease, present at birth and treatable by lung transplants
- Asplenia with cardiovascular anomalies
- Florid cutaneous papillomatosis
- Ectopia cordisBirth defect in which the heart is positioned outside the thorax
- GM1 gangliosidoses
- GM1 gangliosidoses
- Synovial chondromatosis
- Alveolar capillary dysplasiaRare lung disease, present at birth and treatable by lung transplants
- Paroxysmal nocturnal hemoglobinuriaBlood disease in which red blood cells are attacked by the immune system
- Harlequin syndrome
- Idiopathic CD4+ lymphocytopenia
- Giant platelet disorder
- EnterolithSolid mineral mass formed in the gastrointestinal system
- Farber disease
- Dercum's diseaseMedical condition
- Urticaria pigmentosaMost common form of cutaneous mastocytosis
- Waldmann disease
- Rombo syndrome
- Lysosomal acid lipase deficiency