Conditions

Continuously updated · last reviewed Oct 19, 2026

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).

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All 385 Autoimmune 33 Behavioural 13 Cancer 37 Cardiovascular 33 Condition 25 Dental 3 Dermatologic 8 Dermatological 1 Developmental 5 Digestive 19 Endocrine 6 Hematologic 10 Immunologic 7 Infection 1 Infectious 8 Inherited 6 Metabolic 15 Musculoskeletal 18 Neurological 18 Nutritional 1 Ophthalmic 10 Pharmacogenomic 17 Pharmacogenomics 4 Pregnancy 3 Reproductive 4 Respiratory 10 Sensory 5 Trait 53 Urinary 1 Urological 11

25 results in Condition

Condition

Dyshidrosis

Dyshidrosis, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 2,455 cases and 626,220 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.

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Condition

Chondrocalcinosis

Chondrocalcinosis, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 3,282 cases and 625,577 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.

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Condition

Complex Regional/central Pain Syndrome

Complex Regional/central Pain Syndrome, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 3,122 cases and 625,178 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'.

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Condition

Costochondritis

Costochondritis, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 902 cases and 567,630 controls (African American or Afro-Caribbean ancestry, European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.

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Condition

Superficial Keratitis

Superficial Keratitis, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 2,528 cases and 623,139 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.

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Condition

Pyogenic Granuloma

Pyogenic Granuloma, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 1,065 cases and 569,509 controls (African American or Afro-Caribbean ancestry, European ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.

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Condition

Respiratory Insufficiency

Respiratory Insufficiency, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 2,918 cases and 624,478 controls (African American or Afro-Caribbean ancestry, European ancestry, Hispanic or Latin American ancestry). Every figure comes from the studies themselves, gathered by code from the GWAS Catalog and updated as the records grow.

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Condition

Cholelithiasis with Acute Cholecystitis

Cholelithiasis with Acute Cholecystitis, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 2,327 cases and 627,131 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'.

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Condition

Psoriatic Arthropathy

Psoriatic Arthropathy, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 3,723 cases and 628,576 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'.

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Condition

Hypocalcemia

Hypocalcemia, as genome-wide studies have reported it: 8 positions from 1 study, the largest recording 3,109 cases and 624,208 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'.

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Condition

Meningitis

Meningitis, as genome-wide studies have reported it: 10 positions from 2 studies, the largest recording 1,180 cases and 570,786 controls (African American or Afro-Caribbean ancestry, European ancestry). Assembled by code from the GWAS Catalog's records and kept current as positions arrive; every figure is the studies' own.

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Condition

Medication Use as a Genetic Trait

A 2019 UK Biobank study used prescription records themselves, not diagnosis codes, as the trait to study -- and found that genetics behind who takes diabetes or peptic-ulcer drugs mostly recovers the genes already known to cause the underlying diseases.

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Condition

Endometriosis and Depression: Shared Genetics

A reproductive condition and a mood disorder that look unrelated, but a 2020 study built specifically to test the overlap found a real, significant shared genetic architecture between them -- plus an unexpected link to stomach lining abnormality.

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Condition

Diverticular Disease

Small pockets that form in the colon wall, common with age — a 2018 UK Biobank study of over 409,000 people found 39 new risk loci in total, 17 of them in this site's own catalogue, several pointing toward connective-tissue genes.

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Condition

Haemorrhoidal Disease

Swollen, inflamed veins in the lowest part of the rectum or anus, common enough that a 2021 study analyzed 944,133 people at once — finding a genome-wide significant, if individually small, risk variant near BMP8B.

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Condition

Glioma

A brain tumor arising from glial cells, about 50% more common in men than women — three studies from 2009 to 2018 found 6 contributing variants, on this page, including one whose effect differs by sex.

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Condition

Intracranial Aneurysm

A balloon-like weak spot in a brain artery wall, affecting about 2% of people — three studies from 2008 to 2012 found 6 contributing variants, on this page, including one confirmed twice independently.

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Condition

Urolithiasis

A 199,000-person Japanese GWAS more than doubled the number of known genetic risk loci for kidney and urinary stones — 6 of the 14 it found are on this page.

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Condition

Ankylosing Spondylitis

A chronic inflammatory arthritis of the spine and pelvis, driven mainly by HLA-B27 — three separate studies have also found 6 other variants, on this page, each independently.

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Condition

Primary Sclerosing Cholangitis

The largest GWAS of primary sclerosing cholangitis to date found 4 new risk loci and showed the disease is genetically distinct from the inflammatory bowel disease it so often accompanies.

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Questions about conditions on this site

What counts as a "condition" page on this site?

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.

Does MyGeneLog™ diagnose any of these conditions?

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.

Why do some entries say "Trait" instead of a disease category?

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.

How is a variant linked to a condition page?

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.