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Rare Disease Intelligence — 10,888 conditions monitored | Kisho | Kisho

Open data · 12 authoritative sources

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What’s known, in plain language.

Plain-language summaries of 10,888 rare conditions, drawn from MONDO, GeneReviews, ClinVar, FDA, NIH, ClinicalTrials.gov, PubMed, and 5 other public sources. Free, sourced, never gated.

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12

authoritative sources — clinical, regulatory, scientific

10,888

rare conditions, continuously monitored

Daily

updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…

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Showing 1,401-1,420 of 10,888 diseases

autoimmune encephalopathy with parasomnia and obstructive sleep apnea

MONDO:0018489

Autoimmune encephalopathy with parasomnia and obstructive sleep apnea is an extremely rare condition. Because few cases have been documented, detailed...

autoimmune enteropathy

MONDO:0019787

Autoimmune enteropathy is an immune-mediated intestinal disorder that can present as a severe systemic disease in early childhood or as a more isolate...

autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome

MONDO:0013599

Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome is an immune dysregulation disorder that affects the gastroint...

autoimmune enteropathy type 3

MONDO:0015174

autoimmune enteropathy type 3 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

autoimmune glomerulonephritis

MONDO:0030700

Autoimmune glomerulonephritis is an immune-mediated condition in which the body’s own defenses target the kidney’s filtering units, leading to inflamm...

autoimmune hemolytic anemia

MONDO:0020108

Autoimmune hemolytic anemia is an acquired condition in which the immune system mistakenly targets and destroys red blood cells, leading to hemolytic...

autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome

MONDO:0018636

Currently, there is no established genetic basis or inheritance pattern for autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodefi...

autoimmune hemolytic anemia, cold type

MONDO:0016450

Cold autoimmune hemolytic anemia (cAIHA) is characterized by the presence of cold autoantibodies that lead to hemolysis at temperatures below 30°C. Th...

autoimmune hemolytic anemia, warm type

MONDO:0019532

Warm autoimmune hemolytic anemia is the most common form of autoimmune hemolytic anemia. It occurs when the body creates warm autoantibodies that targ...

autoimmune hepatitis

MONDO:0016264

Autoimmune hepatitis is a disorder in which the body’s immune system mistakenly attacks liver cells, leading to inflammation and liver injury. Recogni...

autoimmune hepatitis type 1

MONDO:0005543

Autoimmune hepatitis type 1 (AIH type 1) is characterized by the presence of specific autoantibodies, including antinuclear antibody (ANA) and antismo...

autoimmune hepatitis type 2

MONDO:0021176

Autoimmune hepatitis type 2 is an autoimmune liver disorder characterized by the presence of specific autoantibodies such as anti-liver kidney microso...

autoimmune hepatitis type 3

MONDO:0021177

Autoimmune hepatitis type 3 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

autoimmune hypoparathyroidism

MONDO:0018242

autoimmune hypoparathyroidism is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

autoimmune/inflammatory optic neuropathy

MONDO:0044685

Autoimmune/inflammatory optic neuropathy is a condition that involves inflammation of the optic nerve due to an abnormal immune response. Although a s...

autoimmune interstitial lung disease-arthritis syndrome

MONDO:0014629

Autoimmune interstitial lung disease-arthritis syndrome is a rare disorder that primarily affects the respiratory system and joints. It is characteriz...

autoimmune limbic encephalitis

MONDO:0850097

Autoimmune limbic encephalitis is a rare disorder in which the body’s immune system mistakenly attacks the mesial temporal lobes of the brain. It typi...

autoimmune lymphoproliferative syndrome

MONDO:0017979

Autoimmune lymphoproliferative syndrome (ALPS) is an immune dysregulation disorder in which certain white blood cells grow or survive longer than they...

CTLA4PRKCDFAS+5

autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency

MONDO:0014493

Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsufficiency is an immune-dysregulation disorder in which the body’s defense system becomes...

autoimmune lymphoproliferative syndrome type 1

MONDO:0011158

Autoimmune lymphoproliferative syndrome type 1 (ALPS type 1) is primarily associated with genetic variants in the FAS and FASLG genes, which are cruci...

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