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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 4,361-4,380 of 10,888 diseases
MONDO:0009055
Cutis marmorata telangiectatica congenita is a congenital vascular anomaly characterized by a persistent, marbled pattern of bluish to deep purple ski...
MONDO:0022912
Cutis verticis gyrata mental deficiency is a condition characterized by abnormal scalp folding in association with cognitive challenges. The available...
MONDO:0017640
Cyanide-induced parkinsonism is a neurological syndrome that develops in individuals who have survived an acute cyanide poisoning episode or who have...
MONDO:0018754
Cyanide poisoning occurs when cyanide enters the body, typically through inhalation, ingestion, or skin absorption. It is a life-threatening condition...
MONDO:0008090
Cyclic hematopoiesis is an inherited blood disorder characterized by recurrent periods of low neutrophil counts, which increase the risk of infections...
MONDO:0005725
Cyclosporiasis is an intestinal infection caused by the protozoan Cyclospora cayetanensis, most commonly acquired from consuming contaminated food or...
MONDO:0008058
Cylindrical spirals myopathy is a rare congenital muscle disorder marked by generalized muscle weakness, low muscle tone (hypotonia), myotonia, and cr...
MONDO:0800472
CYP1B1-related glaucoma with or without anterior segment dysgenesis is a form of primary congenital glaucoma that is present at birth. It occurs when...
MONDO:1060107
CYP7B1-related disorder of oxysterol accumulation is a rare condition where oxysterols, which are oxidized cholesterol byproducts, build up in the bod...
MONDO:0007413
Cyprus facial-neuromusculoskeletal syndrome is an exceedingly rare genetic condition that affects many parts of the body. It is characterized by a str...
MONDO:0009058
Cystathioninuria is a metabolic disorder caused by a deficiency of the enzyme cystathionine gamma-lyase, which is encoded by the CTH gene. It is gener...
MONDO:0018408
Cystic echinococcosis is a parasitic infection caused by the larval stage of the tapeworm Echinococcus granulosus. The condition primarily affects the...
MONDO:0015484
Cysticercosis is caused by the larvae of the Taenia solium tapeworm, leading to cyst formation in various tissues, particularly the brain, muscles, an...
MONDO:0009061
Cystic fibrosis is a genetic disorder that primarily affects the respiratory and gastrointestinal systems, leading to abnormally thick mucus secretion...
MONDO:0009062
Cystic fibrosis-gastritis-megaloblastic anemia syndrome is a rare multi-system condition that has been reported in two siblings born to consanguineous...
MONDO:0009761
Cystic hygroma is a benign lymphatic neoplasm that typically arises from the neck, characterized by the formation of fluid-filled cystic spaces due to...
MONDO:0013058
Cystic leukoencephalopathy without megalencephaly is a neurodevelopmental condition marked by non-progressive abnormalities in the brain’s white matte...
MONDO:0020134
Cystic malformation of the posterior fossa is a congenital condition that affects the region at the back of the brain where the cerebellum and brainst...
MONDO:0030604
Cystic partially differentiated nephroblastoma is a rare kidney tumor variant that presents with cystic spaces separated by septa containing immature...
MONDO:0005597
Cystic renal cell carcinoma is a malignant neoplasm of the kidney that arises from the renal tubular epithelium and presents as a fluid-filled mass. A...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.