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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 641-660 of 10,888 diseases
MONDO:0004013
Adult vagina botryoid embryonal rhabdomyosarcoma is a rare type of cancer that develops in the muscle tissues of the vagina. It is a variant of embryo...
MONDO:0004385
Adult xanthogranuloma is a type of xanthogranuloma that is seen in adults. This condition is characterized simply as an occurrence of xanthogranuloma...
MONDO:0003404
Adult yolk sac tumor is a rare type of tumor that develops in adults. It is defined as a yolk sac tumor occurring in an adult, meaning that it is a tu...
MONDO:0015609
Advanced sleep phase syndrome is a very rare circadian rhythm sleep disorder. It is characterized by a very early sleep onset and an early waking time...
MONDO:0011442
Advanced sleep phase syndrome 1 is a rare condition that affects how a person's sleep-wake cycle is regulated. It is characterized by an earlier onset...
MONDO:0014088
Advanced sleep phase syndrome 2 is a condition that affects the body’s natural sleep-wake cycle. This condition is defined as any advanced sleep phase...
MONDO:0014814
Advanced sleep phase syndrome 3 is a condition characterized by a shift in the timing of a person's sleep and wake patterns. People with this conditio...
MONDO:0031044
Advance sleep phase syndrome, familial, 4 is a rare inherited condition that affects the timing of sleep. People with this condition may experience a...
MONDO:0021826
Aerobic Actinomyces infection is a condition caused by an infection with a less common type of Actinomyces bacteria that require oxygen for growth. Th...
MONDO:0100551
AFG2B-related complex neurodevelopmental disorder with motor features and hearing loss is a condition that primarily affects neurological development,...
MONDO:0700372
AFG3L2-related optic atrophy and/or spastic ataxia spectrum is a neurologic condition that affects the optic nerves and motor coordination, and severa...
MONDO:0019733
AFib amyloidosis, also known as familial amyloid nephropathy due to fibrinogen A alpha‐chain variant, is a condition characterized by the deposition o...
MONDO:0003245
Aflatoxin-related hepatocellular carcinoma is a type of liver cancer that develops following exposure to aflatoxin, a potent carcinogen produced by ce...
MONDO:0001262
African histoplasmosis is a fungal infection caused by Histoplasma capsulatum var. Duboisii, a variant predominantly found in parts of Africa. The con...
MONDO:0011012
African iron overload is a condition described primarily in sub-Saharan African populations and is characterized by an excessive accumulation of iron...
MONDO:0000227
African tick-bite fever is an infectious disease caused by the bacterium Rickettsia africae and is transmitted through the bite of infected ticks. It...
MONDO:0015977
Agammaglobulinemia is a condition where there is a decreased level of immunoglobulins in the blood. Immunoglobulins are proteins important for fightin...
MONDO:0030529
Agammaglobulinemia 10, autosomal dominant is a condition that usually begins in early childhood. People with this condition experience recurrent viral...
MONDO:0013287
Agammaglobulinemia 2, autosomal recessive is a rare condition that falls under the group of autosomal agammaglobulinemias. The disease is caused by a...
MONDO:0013288
Agammaglobulinemia 3, autosomal recessive is a rare condition caused by a mutation in the CD79A gene. This disease affects the body’s ability to produ...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.