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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 6,081-6,100 of 10,888 diseases
MONDO:0019317
MONDO:0800114
Follicular bronchiolitis is a lung condition characterized by an abnormal increase in lymphoid tissue within the small airways. It involves a polyclon...
MONDO:0017589
MONDO:0005764
Follicular dendritic cell sarcoma is a low-grade neoplasm that arises from cells resembling follicular dendritic cells and typically affects lymph nod...
MONDO:0013088
Follicular lymphoma, susceptibility to, 1 (FL1) is characterized by a polygenic inheritance pattern, indicating that multiple genes may contribute to...
MONDO:0005032
MONDO:0015808
Folliculotropic mycosis fungoides is a rare variant of mycosis fungoides, a form of cutaneous T-cell lymphoma characterized by folliculotropic infiltr...
MONDO:0023175
Fontaine farriaux blanckaert syndrome is a rare disease. Detailed information about this condition is currently limited in medical literature.
MONDO:0012853
Fontaine progeroid syndrome is a rare premature aging syndrome that affects multiple organ systems, most the skin and craniofacial structures. It is c...
MONDO:0016453
Foodborne botulism is an acquired neuromuscular junction disorder that results from the ingestion of food contaminated with botulinum neurotoxins. Thi...
MONDO:0003109
Foramen magnum meningioma is a tumor affecting the meninges at the foramen magnum, the opening at the base of the skull where the brain transitions in...
MONDO:0023176
MONDO:0009240
Formiminoglutamic aciduria is a metabolic condition that affects the body’s ability to properly process histidine, leading to an accumulation of formi...
MONDO:0009241
Fountain syndrome is an extremely rare multisystem genetic disorder that affects multiple body systems, including hearing, skeletal development, and c...
MONDO:0015378
Fourth branchial cleft anomaly is a congenital developmental malformation that typically presents as a cyst or fistula in the lateral aspect of the ne...
MONDO:0007628
Foveal hypoplasia 1 is an ocular condition characterized by an underdeveloped fovea that is caused by mutations in the PAX6 gene. It affects the centr...
MONDO:0012216
MONDO:0016395
MONDO:0009168
Fowler syndrome is a very rare condition with limited detailed information available. It is known by several names, including encephaloclastic prolife...
MONDO:0100235
FOXC1-related anterior segment dysgenesis is a condition affecting the front part of the eye. It is caused by a mutation in the FOXC1 gene. People wit...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.