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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 4,461-4,480 of 10,888 diseases
MONDO:0004380
Dendritic cell sarcoma is a malignant tumor arising from dendritic cells, which are key components of the immune system. Several recognized subtypes h...
MONDO:0020082
Dendritic cell tumor is a type of neoplasm that arises from cells of the immune system, typically originating in the lymph tissue. The condition is ch...
MONDO:0019207
DEND syndrome is a very rare condition that mainly appears in newborns. It is called a severe form of neonatal diabetes mellitus. In this condition, a...
MONDO:0005502
Dengue disease, commonly known as dengue fever, is caused by the dengue virus and can lead to severe manifestations such as dengue hemorrhagic fever (...
MONDO:0005358
Dengue hemorrhagic fever is a serious condition caused by an infection with the Dengue virus. It starts with a high fever and may be followed by signs...
MONDO:0000248
Dengue shock syndrome is the most severe manifestation of dengue fever and develops as a result of infection with one of the four serotypes of dengue...
MONDO:0022851
Dennis-Fairhurst-Moore syndrome is described as a severe form of Hallermann-Streiff syndrome. This condition has been reported in a single family and...
MONDO:0019736
Dense deposit disease is a chronic kidney disorder characterized by abnormal deposits within the glomerular basement membranes, identified on kidney b...
MONDO:0007435
Dentatorubral-pallidoluysian atrophy, also known as DRPLA, is a rare subtype of type I autosomal dominant cerebellar ataxia that primarily affects the...
MONDO:0015612
Dent disease is a rare genetic kidney condition that affects the renal tubules, the tiny tubes in the kidneys that help remove waste and extra water f...
MONDO:0010225
Dent disease type 1 is a rare genetic disorder that mainly affects the kidneys. It is a form of Dent disease with predominantly renal manifestations....
MONDO:0010359
Dent disease type 2 is a form of Dent disease that shows the kidney problems seen in Dent disease type 1 along with additional features affecting othe...
MONDO:0015613
Dentin dysplasia is a hereditary disorder affecting the structure of dentin, leading to abnormal tooth development and root formation. It is classifie...
MONDO:0007438
Dentin dysplasia-sclerotic bones syndrome is a rare condition characterized by abnormal development of dentin in the teeth and excessive hardening of...
MONDO:0007436
Dentin dysplasia type I is a rare dental condition characterized by teeth with abnormally short or even absent roots, which can compromise tooth stabi...
MONDO:0007437
Dentin dysplasia type II is an uncommon dental condition characterized by largely normal tooth roots but abnormal appearance of the primary dentition....
MONDO:0019102
Dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome is a condition that affects multiple organ systems, most dental...
MONDO:0007442
Dentinogenesis imperfecta type 3 (DGI-3) is a severe inherited disorder affecting the structure and appearance of teeth. It is characterized by opales...
MONDO:0008682
Denys-Drash syndrome (DDS) is a rare condition that mainly affects the urogenital system. It is characterized by a specific kidney problem called diff...
MONDO:0002526
Dermal unilateral segmental cavernous angioma is a localized vascular anomaly of the skin characterized by a segmentally distributed cluster of dilate...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.