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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.
Kisho provides public health information only — not medical advice. Always consult your healthcare provider.
12
authoritative sources — clinical, regulatory, scientific
10,888
rare conditions, continuously monitored
Daily
updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…
Showing 1,161-1,180 of 10,888 diseases
MONDO:0018093
Arbovirus fever is a condition caused by arbovirus infections transmitted by vector insects such as mosquitoes and ticks. Although the illness can, in...
MONDO:0008812
AREDYLD syndrome is a multisystem condition characterized by features including lipoatrophy, diabetes mellitus, generalized hypotrichosis, ectodermal...
MONDO:0015100
Aregenerative anemia is a condition characterized by an insufficient production of blood cells, leading to various symptoms of anemia. The underlying...
MONDO:0005651
Arenavirus hemorrhagic fever is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0017874
Argentine hemorrhagic fever (AHF), also known as Argentinian hemorrhagic fever or Junin hemorrhagic fever, is an acute viral hemorrhagic illness that...
MONDO:0008814
Arginase deficiency is a metabolic disorder affecting the urea cycle, primarily involving the enzyme produced by the ARG1 gene on chromosome 6. It is...
MONDO:0008815
Argininosuccinic aciduria is a metabolic disorder affecting the urea cycle that disrupts the body’s ability to remove ammonia, a toxic byproduct of pr...
MONDO:0018952
Argyria is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by irrev...
MONDO:0011323
Arhinia, choanal atresia, and microphthalmia is a very rare multisystem condition that primarily affects development of the nose, eyes, and midface. I...
MONDO:1040065
ARL6-related ciliopathy is a condition classified among disorders of the cellular cilia, which are hair-like structures that play a crucial role in ce...
MONDO:0010284
Armfield syndrome is an X-linked intellectual disability disorder primarily affecting males and characterized by cognitive impairment, short stature,...
MONDO:0021921
Arnold stickler bourne syndrome is a condition that appears to affect multiple organ systems, although specific details about the affected systems hav...
MONDO:0013301
Aromatase deficiency is an inherited endocrine condition that interferes with the body’s ability to convert androgens into estrogens, affecting reprod...
MONDO:0007690
Aromatase excess syndrome is a rare genetic endocrine condition characterized by increased estrogen levels due to elevated extraglandular aromatase ac...
MONDO:0012084
Aromatic L-amino acid decarboxylase deficiency (often called AADC deficiency) is a very rare neurometabolic condition that disrupts the brain’s abilit...
MONDO:0015237
Arrhinia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is characterized by the...
MONDO:0011581
Arrhythmogenic cardiomyopathy with wooly hair and keratoderma is a very rare inherited disorder that affects both the heart and the skin-hair system....
MONDO:0016587
Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a heart muscle disease that primarily affects the right ventricle, where normal myocardial t...
MONDO:0007152
Arrhythmogenic right ventricular dysplasia 1 is a type of cardiomyopathy that mainly affects the right ventricle. It is caused by mutations in the TGF...
MONDO:0012434
Arrhythmogenic right ventricular dysplasia 10 is a cardiac condition that primarily affects the right ventricle, leading to disturbances in the heart'...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.