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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 7,461-7,480 of 10,888 diseases

hypothyroidism due to TSH receptor mutations

MONDO:0010142

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

hypothyroidism due to TSH receptor mutations

hypotonia, ataxia, and delayed development syndrome

hypotonia-cystinuria syndrome

hypotonia-failure to thrive-microcephaly syndrome

hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities

hypotonia, infantile, with psychomotor retardation and characteristic facies

hypotonia, infantile, with psychomotor retardation and characteristic facies 1

hypotonia, infantile, with psychomotor retardation and characteristic facies 2

hypotonia, infantile, with psychomotor retardation and characteristic facies 3

hypotonia with lactic acidemia and hyperammonemia

hypotrichosis 1

hypotrichosis 10

hypotrichosis 11

hypotrichosis 12

hypotrichosis 13

hypotrichosis 14

hypotrichosis 2

hypotrichosis 3

hypotrichosis 4

hypotrichosis 5

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