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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 9,501-9,520 of 10,888 diseases

megalencephalic leukoencephalopathy with subcortical cysts

MONDO:0011391

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

megalencephalic leukoencephalopathy with subcortical cysts

megalencephalic leukoencephalopathy with subcortical cysts 1

megalencephalic leukoencephalopathy with subcortical cysts 2A

megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability

megalencephaly

megalencephaly, autosomal dominant

megalencephaly-capillary malformation-polymicrogyria syndrome

megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1

megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2

megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3

megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome

megalencephaly-severe kyphoscoliosis-overgrowth syndrome

megaloblastic anemia

megaloblastic anemia, folate-responsive

megaloblastic anemia-immunodeficiency due to folate transporter 1 deficiency

megalocornea-intellectual disability syndrome

megalodactyly

MEGF10-related myopathy

MEGF8-related Carpenter syndrome

MEHMO syndrome

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