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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 7,261-7,280 of 10,888 diseases
MONDO:0007757
Hyperkeratosis-hyperpigmentation syndrome is a very rare skin condition characterized by tiny hyperpigmented spots on sun-exposed areas and mild punct...
MONDO:0007756
Hyperkeratosis lenticularis perstans is a skin condition characterized by persistent, keratotic areas that can appear as small, rough papules. It is a...
MONDO:0011470
Hyperlipidemia, combined, 2 is a metabolic condition that affects the regulation of blood fats, including cholesterol and triglycerides. It is recogni...
MONDO:0013533
Hyperlipidemia due to hepatic triglyceride lipase deficiency is a rare genetic disorder of lipid metabolism that results in markedly elevated levels o...
MONDO:0007759
Familial combined hyperlipidemia, LPL related is an inherited metabolic condition that primarily affects lipid regulation in the body. This condition...
MONDO:0014412
Hyperlipoproteinemia, type 1D is a rare inherited lipid disorder caused by mutations in the GPIHBP1 gene that disrupt normal lipid metabolism. This co...
MONDO:0018473
Hyperlipoproteinemia type 3 is a combined hyperlipidemia characterized by elevated cholesterol and triglyceride levels carried by intermediate density...
MONDO:0007762
Hyperlipoproteinemia type V is a severe lipid disorder characterized by an abnormal elevation of both plasma chylomicrons and very-low-density lipopro...
MONDO:0009388
Hyperlysinemia is a metabolic disorder characterized by abnormally high levels of lysine in the blood and cerebrospinal fluid. This condition results...
MONDO:0009389
MONDO:0000214
Hypermanganesemia with dystonia is a condition that primarily affects the nervous system, particularly manifesting as movement difficulties due to dys...
MONDO:0014864
Hypermanganesemia with dystonia 2 is a rare neurologic condition marked by impaired movement and difficulties with feeding, primarily due to dystonia...
MONDO:0013404
Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase is a very rare metabolic disorder that primarily affects neuromuscular developm...
MONDO:0009395
MONDO:0007765
MONDO:0007767
Hyperparathyroidism 1 is an inherited condition primarily affecting the parathyroid glands, which play a key role in regulating calcium levels in the...
MONDO:0007768
Hyperparathyroidism 2 with jaw tumors is an inherited condition that primarily affects the parathyroid glands and jaw, with additional involvement of...
MONDO:0012406
MONDO:0024570
Hyperparathyroidism 4 is a familial form of isolated hyperparathyroidism caused by mutations in the GCM2 gene that affect the parathyroid glands. This...
MONDO:0044350
Hyperparathyroidism, primary, caused by water clear cell hyperplasia is an endocrine condition affecting the parathyroid glands and their regulation o...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.