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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 5,261-5,280 of 10,888 diseases

Emery-Dreifuss muscular dystrophy 3, autosomal recessive

MONDO:0014676

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

Emery-Dreifuss muscular dystrophy 3, autosomal recessive

Emery-Dreifuss muscular dystrophy 4, autosomal dominant

Emery-Dreifuss muscular dystrophy 5, autosomal dominant

Emery-Dreifuss muscular dystrophy 6, X-linked

Emery-Dreifuss muscular dystrophy 7, autosomal dominant

Emery-Nelson syndrome

EMILIN-1-related connective tissue disease

emphysematous cholecystitis

empty nose syndrome

EN1-related dorsoventral syndrome

encapsulated thymoma

encephalitis lethargica

encephalitozoonosis

encephaloclastic disorder

encephalocraniocutaneous lipomatosis

encephalopathy due to beta-mercaptolactate-cysteine disulfiduria

encephalopathy due to defective mitochondrial and peroxisomal fission 2

encephalopathy due to GLUT1 deficiency

encephalopathy due to hydroxykynureninuria

encephalopathy due to mitochondrial and peroxisomal fission defect

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