Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
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 8,001-8,020 of 10,888 diseases
MONDO:0030916
MONDO:0030917
MONDO:0030918
MONDO:0030919
MONDO:0030920
Intellectual disability, autosomal dominant 54 is a neurodevelopmental disorder that primarily affects cognitive and developmental functions. The cond...
MONDO:0030921
Intellectual disability, autosomal dominant 55, with seizures is a neurodevelopmental disorder primarily affecting the central nervous system. It is c...
MONDO:0030922
Intellectual disability, autosomal dominant 56, also known as CLTC-related intellectual disability, is a neurodevelopmental disorder that primarily af...
MONDO:0054837
MONDO:0020847
Intellectual disability, autosomal dominant 58 is a neurodevelopmental condition that primarily affects cognitive and developmental functioning, along...
MONDO:0013509
Intellectual disability, autosomal dominant 6 is a neurodevelopmental condition characterized by significant cognitive impairment, seizures, and globa...
MONDO:0013656
Intellectual disability, autosomal dominant 9 is a very rare neurodevelopmental condition caused by pathogenic variants in the KIF1A gene. It typicall...
MONDO:0009580
Intellectual disability, autosomal recessive 1 is a neurodevelopmental condition that primarily affects cognitive functioning. It is caused by mutatio...
MONDO:0012618
MONDO:0012619
MONDO:0012612
Intellectual disability, autosomal recessive 12 is an inherited condition primarily affecting neurodevelopment and cognitive function. It is caused by...
MONDO:0013173
Intellectual disability, autosomal recessive 13 is a neurodevelopmental condition caused by mutations in the TRAPPC9 gene. This condition is character...
MONDO:0013528
MONDO:0013629
MONDO:0013651
Intellectual disability, autosomal recessive 18 is a neurodevelopmental condition caused by mutations in the MED23 gene. This disorder primarily affec...
MONDO:0013705
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.