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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 6,441-6,460 of 10,888 diseases

glycerol kinase deficiency, juvenile form

MONDO:0017295

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

glycerol kinase deficiency, juvenile form

glyceronephosphate O-acyltransferase deficiency

glycine encephalopathy

glycine encephalopathy 1

glycine encephalopathy 2

glycine N-methyltransferase deficiency

glycogen storage disease due to acid maltase deficiency, infantile onset

glycogen storage disease due to acid maltase deficiency, late-onset

glycogen storage disease due to aldolase A deficiency

glycogen storage disease due to glucose-6-phosphatase deficiency type IA

glycogen storage disease due to GLUT2 deficiency

glycogen storage disease due to glycogen branching enzyme deficiency

glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form

glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form

glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form

glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form

glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form

glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form

glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form

glycogen storage disease due to lactate dehydrogenase deficiency

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