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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.
Kisho provides public health information only — not medical advice. Always consult your healthcare provider.
12
authoritative sources — clinical, regulatory, scientific
10,888
rare conditions, continuously monitored
Daily
updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…
Showing 7,961-7,980 of 10,888 diseases
MONDO:0032770
MONDO:0032870
MONDO:0030849
MONDO:0032864
MONDO:0060763
Intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities is a neurodevelopmental condition that primarily af...
MONDO:0026723
MONDO:0859086
Intellectual developmental disorder, X-linked 110 is a neurodevelopmental condition that primarily affects the nervous system, with severe intellectua...
MONDO:0957203
MONDO:0957496
MONDO:0958200
MONDO:0975828
MONDO:0026733
MONDO:0024772
Intellectual developmental disorder, X-linked, syndromic, Pilorge type is a neurodevelopmental condition primarily affecting individuals assigned male...
MONDO:0013353
MONDO:0007974
Intellectual disability, autosomal dominant 1 is a neurodevelopmental condition characterized by severe developmental and cognitive delays, distinctiv...
MONDO:0013657
Intellectual disability, autosomal dominant 10 is a neurodevelopmental condition primarily characterized by moderate cognitive impairment. It results...
MONDO:0013658
MONDO:0013805
MONDO:0013819
Intellectual disability, autosomal dominant 14 is a developmental condition in which individuals exhibit a characteristic constellation of physical an...
MONDO:0013820
Intellectual disability, autosomal dominant 15, a variant of Coffin-Siris syndrome caused by a mutation in the SMARCB1 gene, primarily affects neurode...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.