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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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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

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

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Showing 10,321-10,340 of 10,888 diseases

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5

MONDO:0013157

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

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9

muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type B, 15

muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1

muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14

muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2

muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3

muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4

muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8

muscular dystrophy-dystroglycanopathy, type A

muscular dystrophy-dystroglycanopathy, type B

muscular dystrophy-dystroglycanopathy type B5

muscular dystrophy-dystroglycanopathy type B6

muscular dystrophy-dystroglycanopathy, type C

muscular dystrophy, Hemizygous lethal type

muscular dystrophy, limb-girdle, autosomal dominant

muscular dystrophy, limb-girdle, autosomal dominant 4

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