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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 5,481-5,500 of 10,888 diseases
MONDO:0012729
Erythrocytosis, familial, 4 is a hereditary blood disorder characterized by an abnormally high red blood cell mass. The condition is caused by mutatio...
MONDO:0033483
Erythrocytosis, familial, 5 is a form of familial polycythemia that arises from a mutation in the EPO gene, a key regulator of red blood cell producti...
MONDO:0054801
Erythrocytosis, familial, 6 is a condition that primarily affects the blood system, characterized by an abnormally high concentration of hemoglobin an...
MONDO:0054802
Familial erythrocytosis, familial, 7 is a genetic condition characterized by an increase in red blood cell production linked to changes in the alpha-g...
MONDO:0017787
Erythroderma desquamativum, also known by names such as Leiner disease and Leiner-Moussous desquamative erythroderma, is a disorder primarily affectin...
MONDO:0020703
Erythroid neoplasm is a type of malignant tumor that arises from the erythroid lineage of blood cells. Research has implicated abnormalities in the JA...
MONDO:0019270
Erythrokeratoderma is an umbrella term for a group of rare genetic skin disorders marked by well-demarcated plaques of reddened, dry, and thickened sk...
MONDO:0017836
MONDO:0017851
Erythrokeratodermia variabilis is a rare genetic chronic skin disorder characterized by hyperkeratosis and transient erythema. It primarily affects th...
MONDO:0033010
Erythrokeratodermia variabilis et progressiva 1 is a genetic skin condition primarily characterized by persistent redness and thickening of the skin....
MONDO:0033012
Erythrokeratodermia variabilis et progressiva 2 is a genetic skin condition characterized primarily by the persistent presence of skin plaques and ery...
MONDO:0033013
Erythrokeratodermia variabilis et progressiva 3 is a genetic skin disorder that primarily affects the epidermis, with characteristic changes such as r...
MONDO:0033014
Erythrokeratodermia variabilis et progressiva 4 is a skin disorder characterized by abnormal thickening and redness of the skin. It is caused by patho...
MONDO:0033015
MONDO:0032801
Erythrokeratodermia variabilis et progressiva 6 is a skin condition characterized by red, inflamed plaques that are a consistent and defining feature...
MONDO:0030941
Erythrokeratodermia variabilis et progressiva 7 (EKVP7) is a condition affecting the skin and its appendages, characterized by distinctive changes in...
MONDO:0859598
MONDO:0007573
MONDO:0001676
Erythropoietic protoporphyria is a rare congenital metabolic disorder resulting from an inborn error in the porphyrin-heme biosynthesis pathway. The c...
MONDO:0017231
Erythropoietic uroporphyria associated with myeloid malignancy is a very rare condition, affecting fewer than 1 in 1,000,000 people. Although detailed...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.