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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 6,821-6,840 of 10,888 diseases
MONDO:0018492
Hereditary clear cell renal cell carcinoma is an inherited form of kidney cancer that presents as a malignant epithelial neoplasm, most commonly in th...
MONDO:0019943
MONDO:0007369
Hereditary coproporphyria is a form of acute hepatic porphyria that primarily disrupts heme synthesis and manifests through neuro-visceral attacks, wi...
MONDO:0012143
Hereditary cryohydrocytosis with reduced stomatin is a very rare multisystem condition that affects blood, the central nervous system, and other organ...
MONDO:0015547
Hereditary dementia is an inherited form of dementia characterized by progressive cognitive decline resulting from a genomic modification. Variants in...
MONDO:0007648
Hereditary diffuse gastric adenocarcinoma is a form of stomach cancer that originates in the lining of the stomach and is characterized by the presenc...
MONDO:0003847
Hereditary disease refers to a group of conditions caused by genetic modifications that are passed from parent to child. This condition arises from va...
MONDO:0015514
Hereditary endocrine growth disease is a disorder that affects the regulation of growth through the endocrine system. Although detailed information ab...
MONDO:0021026
Hereditary epidermal appendage anomaly is a genetic condition that affects the skin’s structures, which include components such as hair, nails, and sw...
MONDO:0016227
Hereditary episodic ataxia is a group of neurological disorders marked by recurrent episodes of loss of balance, vertigo, and impaired coordination, o...
MONDO:0004166
MONDO:0009238
Hereditary folate malabsorption is an inherited disorder affecting the transport of folate, leading to a systemic and central nervous system deficienc...
MONDO:0009249
Hereditary fructose intolerance is a metabolic disorder that results from a deficiency of the enzyme hepatic fructose-1-phosphate aldolase, caused by...
MONDO:0018502
Hereditary gastric cancer describes a familial tendency to develop cancer of the stomach, often evident when two or more affected relatives are observ...
MONDO:0008588
MONDO:0016070
MONDO:0018174
Hereditary glaucoma is a group of rare eye disorders characterized by elevated intraocular pressure and changes in the optic nerve head that can lead...
MONDO:0030038
Hereditary glaucoma, primary closed-angle is an ocular condition that involves increased pressure within the eye, potentially leading to damage of the...
MONDO:0006507
Hereditary hemochromatosis is an inherited metabolic disorder characterized by excessive iron accumulation in the body's tissues. Variants in the HFE,...
MONDO:0957097
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.