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Rare Disease Intelligence — 10,888 conditions monitored | Kisho | Kisho

Open data · 12 authoritative sources

Find your disease.
What’s known, in plain language.

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.

Search by:Disease•Gene•Symptom•Treatment•PAG•OMIM/Orphanet ID

Commonly searched:Cystic Fibrosis Duchenne Huntington's ALS Sickle Cell

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Plain language
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Kisho provides public health information only — not medical advice. Always consult your healthcare provider.

authoritative sources — clinical, regulatory, scientific

10,888

rare conditions, continuously monitored

Daily

updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…

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Showing 7,201-7,220 of 10,888 diseases

hyperbilirubinemia, shunt, primary

MONDO:0009382

Find your disease.What’s known, in plain language.

hyperbilirubinemia, shunt, primary

hyperbiliverdinemia

hypercalcemia, infantile

hypercalcemia, infantile, 1

hypercalcemia, infantile, 2

hypercalcemic sarcoidosis

hypercalcemic type ovarian small cell carcinoma

hypercalciuria, absorptive, 1

hypercalciuria, absorptive, 2

hypercarotenemia and vitamin A deficiency, autosomal recessive

hypercholanemia, familial

hypercholanemia, familial 1

hypercholanemia, familial, 2

hypercholesterolemia, autosomal dominant, 3

hypercholesterolemia, autosomal dominant, type B

hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency

hypercholesterolemia, familial, 1

hypercholesterolemia, familial, 4

hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency

hyperdibasic aminoaciduria type 1

Find your disease.
What’s known, in plain language.