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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 4,301-4,320 of 10,888 diseases
MONDO:0008494
Cryohydrocytosis is a rare, hereditary hemolytic anemia caused by a red blood cell membrane anomaly. It is associated with a leakage of potassium from...
MONDO:0016168
Cryopyrin-associated periodic syndrome (CAPS) is an autoinflammatory condition characterized by recurrent systemic inflammatory episodes in the absenc...
MONDO:0005723
Cryptococcal meningitis is an infection of the membranes surrounding the brain and spinal cord caused by the encapsulated yeast Cryptococcus neoforman...
MONDO:0005724
Cryptococcosis is an acute or chronic infection caused by the fungus Cryptococcus neoformans, which can present as a localized or disseminated infecti...
MONDO:0015585
Cryptogenic late-onset epileptic spasms is a rare epilepsy syndrome that typically begins after the first year of life and is characterized by cluster...
MONDO:0018765
Cryptogenic multifocal ulcerous stenosing enteritis is a very rare gastrointestinal condition that is characterized by the development of multiple ulc...
MONDO:0015264
Cryptogenic organizing pneumonia (COP) is a form of idiopathic interstitial pneumonia that affects the lung tissue, where the small airways and alveol...
MONDO:0007409
Cryptomicrotia-brachydactyly-excess fingertip arch syndrome is a condition characterized by distinctive malformations of the ears and digits. Affected...
MONDO:0020153
Cryptophthalmia is a congenital condition characterized by a continuous layer of skin that extends over the eyeballs and the absence of eyelids and th...
MONDO:0015473
Cryptorchidism-arachnodactyly-intellectual disability syndrome is a very rare condition that involves multiple congenital anomalies affecting the skel...
MONDO:0014082
Cryptosporidiosis-chronic cholangitis-liver disease syndrome is an ultra-rare multisystem disorder characterized by significant immune dysfunction and...
MONDO:0008893
C syndrome is a rare condition that affects many parts of the body. It is known for causing an abnormal head shape called trigonocephaly due to the ea...
MONDO:0100256
CTNNA1-related diffuse gastric and lobular breast cancer syndrome is a hereditary condition. It is linked to changes in the CTNNA1 gene that increase...
MONDO:0800465
CTSC-related disorder is a group of conditions caused by changes in the CTSC gene. These disorders include papillon-Lefevre syndrome, which is known f...
MONDO:0043982
Cubital tunnel syndrome is a condition characterized by the compression of the ulnar nerve at the elbow, where the nerve passes through a narrow passa...
MONDO:0011883
Curly hair - acral keratoderma - caries syndrome is an extremely rare ectodermal dysplasia syndrome. People with this condition often experience prema...
MONDO:0008305
Currarino syndrome is a rare congenital condition that is defined by a specific triad of abnormalities. People with this condition typically have an a...
MONDO:0011134
Curry-Jones syndrome is a condition that affects the development of the head, brain, hands, feet, skin, eyes, and gut. People with this condition may...
MONDO:0009050
Cushing disease due to pituitary adenoma is a form of ACTH-dependent Cushing syndrome. It is caused by a small, benign tumor on the pituitary gland th...
MONDO:0018912
Cushing syndrome is an endocrine disorder characterized by prolonged exposure to high levels of glucocorticoids, which can arise from the body’s own o...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.