Each page covers one condition properly: what it actually is and what it feels like, what causes it, how common it really is and in whom, and how it's diagnosed — followed by the specific variants with a replicated link to it, and, where the research supports it, how genetics can change the way a medicine behaves.
Written in two registers so one page serves both readers: plain language first, then a clinical detail section with the precise terminology, effect sizes and diagnostic thresholds. Every claim is sourced from freely-available published research and cited on the page, so you can check us — or hand the page to your doctor. 385 conditions so far, growing continuously, and free to reuse with attribution (CC BY 4.0).
Cutaneous Squamous Cell Carcinoma, as genome-wide studies have reported it: 4 positions from 2 studies, the largest recording 16,407 cases and 762,486 controls (European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → DigestiveInfantile Hypertrophic Pyloric Stenosis, as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 1,395 cases and 4,438 controls. Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → DermatologicErythematosquamous Dermatosis, as genome-wide studies have reported it: 3 positions from 1 study, the largest recording 38,469 cases and 568,738 controls (African American or Afro-Caribbean ancestry, Hispanic or Latin American ancestry, East Asian ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → DermatologicDermatophytosis, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 256,822 European, African, Hispanic or Latin American and Asian ancestry cases, 1,372,501 European, African, Hispanic or Latin American and Asian ancestry controls. Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → DigestiveGastroesophageal Reflux Disease, as genome-wide studies have reported it: 12 positions from 2 studies, the largest recording 129,080 cases and 473,524 controls (European ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → DigestiveGastric Ulcer, as genome-wide studies have reported it: 4 positions from 3 studies, the largest recording 28,682 cases and 867,208 controls (Japanese ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → MusculoskeletalFibromyalgia, as genome-wide studies have reported it: 6 positions from 2 studies, the largest recording 2,563,755 individuals (European ancestry, African ancestry, South Asian ancestry, Hispanic or Latin American ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → DermatologicSeborrheic Keratosis, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 97,056 cases and 472,839 controls (African American or Afro-Caribbean ancestry, Hispanic or Latin American ancestry, East Asian ancestry, European ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → InfectiousCOVID-19 with Respiratory Failure Requiring Mechanical Ventilation, as genome-wide studies have reported it: 3 positions from 1 study, the largest recording 13,052 cases and 1,438,150 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → RespiratoryPharyngeal Disease, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 33,157 cases and 199,208 controls. Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.
Read more → DigestiveIrritable Bowel Syndrome, as genome-wide studies have reported it: 10 positions from 4 studies, the largest recording 68,267 cases and 860,556 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → MusculoskeletalSpinal Stenosis, as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 61,730 cases and 545,165 controls (African American or Afro-Caribbean ancestry, Hispanic or Latin American ancestry, East Asian ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → MusculoskeletalCarpal Tunnel Syndrome, as genome-wide studies have reported it: 18 positions from 3 studies, the largest recording 48,843 cases and 1,190,837 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → OphthalmicFuchs's Corneal Dystrophy, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 3,655 cases and 254,909 controls (European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → UrologicalClassic Bladder Exstrophy, as genome-wide studies have reported it: 4 positions from 2 studies, the largest recording 628 cases and 7,352 controls (European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → ReproductivePelvic Organ Prolapse, as genome-wide studies have reported it: 8 positions from 2 studies, the largest recording 28,857 cases and 622,916 controls (Japanese ancestry, European ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → MetabolicFamilial Combined Hyperlipidemia Defined by Consensus Criteria, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 39,961 cases and 309,261 controls. Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → CardiovascularCardiomyopathy, as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 7,053 cases and 111,507 controls (African American or Afro-Caribbean ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more → DigestiveUmbilical Hernia, as genome-wide studies have reported it: 63 positions from 3 studies, the largest recording 20,188 cases and 602,677 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Built from the GWAS Catalog's records and rebuilt when a new position is reported; the figures are the studies'.
Read more → CardiovascularHypertrophic Cardiomyopathy, as genome-wide studies have reported it: 28 positions from 4 studies, the largest recording 890 cases and 666,965 controls (European ancestry, East Asian ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.
Read more →Showing 20 of 385 · page 4 of 20
One diagnosed condition or measurable trait covered properly: what it actually is, what causes it, how common it is, how it is diagnosed, and the specific variants with a replicated link to it — every claim sourced from published research.
No. Every page here is informational, not a diagnosis. A result should be discussed with a doctor or a licensed genetic counselor, never acted on alone.
Because they are not disorders. Height, ABO blood group and a handful of others describe a measurable characteristic with nothing to diagnose — "Trait" says so plainly instead of implying a disease that is not one.
Only after a replicated association in published research, verified against the primary study rather than a gene name or a marketing claim — the same discipline the variant pages themselves follow.