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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 221-240 of 10,888 diseases
MONDO:0600017
Acinar dysplasia caused by mutation in FGF10 is a rare condition where a change in the FGF10 gene leads to abnormal development of acinar tissue. This...
MONDO:0600018
Acinar dysplasia caused by a mutation in the FGFR2 gene is a condition that affects the acinar cells. Acinar cells are important for the function of c...
MONDO:0600019
Acinar dysplasia caused by a mutation in the TBX4 gene is a rare condition. In this disorder, the normal structures of the acinar cells, which are inv...
MONDO:0003892
Acinar lung adenocarcinoma is a morphologic variant of lung adenocarcinoma. This condition is characterized by the presence of acinar structures, whic...
MONDO:0018442
Acitretin/Etretinate embryopathy is a disorder that occurs when a pregnant person is exposed to the medications acitretin or etretinate during the fir...
MONDO:0008706
Ackerman syndrome is a condition primarily affecting dental and ocular structures, characterized by features such as pyramidal molar roots and taurodo...
MONDO:1060120
ACO2-related optic atrophy with or without extraocular features is a disorder primarily affecting the optic nerves, sometimes accompanied by additiona...
MONDO:0001569
Acoustic neuroma, also known as vestibular schwannoma, is a benign tumor that arises from Schwann cells, which are responsible for the myelin sheath s...
MONDO:0045023
Acquired adrenogenital syndrome is a form of adrenogenital syndrome that develops during an individual’s lifetime rather than being present from birth...
MONDO:0017617
Acquired adult-onset immunodeficiency is a condition in which the immune system becomes weakened during adulthood. This means that people with this co...
MONDO:0021758
Acquired agranulocytosis is a condition in which the body’s immune system mistakenly targets and reduces a type of white blood cell called granulocyte...
MONDO:0019543
Acquired aneurysmal subarachnoid hemorrhage is a serious and life-threatening neurologic condition that occurs when an intracranial aneurysm ruptures...
MONDO:0019624
Acquired angioedema is a condition where people experience temporary and repeated swellings in the skin and mucosal tissues. This can lead to noticeab...
MONDO:0015056
Acquired angioedema type 1 (AAE 1) is a type of acquired angioedema that is marked by episodes of sudden swelling. These episodes can affect the subcu...
MONDO:0015055
Acquired angioedema type 2 (AAE2) is a form of angioedema that develops later in life. It is characterized by sudden swelling in the layers beneath th...
MONDO:0033948
Information about overview is currently limited for this condition.
MONDO:0015610
Acquired aplastic anemia is a type of aplastic anemia that develops during a person’s lifetime. This condition involves a failure of the bone marrow t...
MONDO:0016593
Acquired ataxia is a type of ataxia that develops during a person's lifetime. Unlike inherited forms of ataxia, this condition is not present at birth...
MONDO:0019846
Acquired central diabetes insipidus (acquired CDI) is a disorder where the body produces less vasopressin (AVP), a hormone that helps control water ba...
MONDO:0020599
Acquired coagulation factor deficiency is a rare condition where a person has a lower level of a blood clotting factor without a genetic cause. This d...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.