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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 6,981-7,000 of 10,888 diseases

hereditary spastic paraplegia 75

MONDO:0014729

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

hereditary spastic paraplegia 75

hereditary spastic paraplegia 77

hereditary spastic paraplegia 8

hereditary spastic paraplegia 9A

hereditary spherocytosis type 1

hereditary spherocytosis type 2

hereditary spherocytosis type 3

hereditary spherocytosis type 4

hereditary spherocytosis type 5

hereditary stomatocytosis

hereditary thermosensitive neuropathy

hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1

hereditary thrombocytopenia and hematologic cancer predisposition syndrome

hereditary thrombocytosis with transverse limb defect

hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency

hereditary thrombophilia due to congenital protein C deficiency

hereditary thrombophilia due to congenital protein S deficiency

hereditary Wilms tumor

hereditary xanthinuria

heritable pulmonary arterial hypertension

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