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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

Daily

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

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Showing 401-420 of 10,888 diseases

acute motor and sensory axonal neuropathy

MONDO:0020348

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

acute motor and sensory axonal neuropathy

acute motor axonal neuropathy

acute myeloblastic leukemia with maturation

acute myeloblastic leukemia without maturation

acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent

acute myeloid leukemia and myelodysplastic syndromes related to radiation

acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor

acute myeloid leukemia, biallelic CEBPA gene mutation

acute myeloid leukemia, CEBPA gene mutation

acute myeloid leukemia, del(13q14-q21)

acute myeloid leukemia, del(5q31-q32)

acute myeloid leukemia, der12p

acute myeloid leukemia, FLT3 internal tandem duplication

acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation

acute myeloid leukemia, GATA1 gene mutation

acute myeloid leukemia, inv(16)(p13.1;q22)

acute myeloid leukemia, inv(16)(p13.3;q24.3)

acute myeloid leukemia, inv(3)(q21.3;q26.2)

acute myeloid leukemia, KIT exon 17 mutation

acute myeloid leukemia, KIT exon 8 mutation

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