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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 421-440 of 10,888 diseases

acute myeloid leukemia, KIT gene mutation

MONDO:0100420

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

acute myeloid leukemia, KIT gene mutation

acute myeloid leukemia, KRAS gene mutation

acute myeloid leukemia, loss of chromosome 17p

acute myeloid leukemia, MLL gene rearrangement

acute myeloid leukemia, monoallelic CEBPA gene mutation

acute myeloid leukemia, Monosomy 5

acute myeloid leukemia, Monosomy 7

acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive

acute myeloid leukemia, NRAS gene mutation

acute myeloid leukemia, PTPN11 gene mutation

acute myeloid leukemia, RUNX1 gene mutation

acute myeloid leukemia, t(10;11)(p11.2;q23)

acute myeloid leukemia, t(10;11)(p12;q23)

acute myeloid leukemia, t(11;15)(p15;q35)

acute myeloid leukemia, t(11;17)

acute myeloid leukemia, t(11;19)(q23.3;p13.3)

acute myeloid leukemia, t(11;19)(q23;p13)

acute myeloid leukemia, t(11;19)(q23;p13.1)

acute myeloid leukemia, t(1;11)(q21;q23)

acute myeloid leukemia, t(1;22)

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