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

11 results in Urological

Urological

Dysplasia of Prostate

Dysplasia of Prostate, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 1,376 cases and 518,488 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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Urological

Glomerulonephritis

Glomerulonephritis, as genome-wide studies have reported it: 5 positions from 1 study, the largest recording 2,204 cases and 629,134 controls (African American or Afro-Caribbean ancestry, European 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.

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Urological

Nephritis and Nephropathy with Pathological Lesion

Nephritis and Nephropathy with Pathological Lesion, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 2,623 cases and 627,347 controls (African American or Afro-Caribbean ancestry, European 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.

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Urological

Non-proliferative Glomerulonephritis

Non-proliferative Glomerulonephritis, as genome-wide studies have reported it: 6 positions from 1 study, the largest recording 967 cases and 571,873 controls (African American or Afro-Caribbean ancestry, European 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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Urological

Chronic Glomerulonephritis, NOS

Chronic Glomerulonephritis, NOS, as genome-wide studies have reported it: 16 positions from 1 study, the largest recording 667 cases and 571,939 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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Urological

Peyronie's Disease

Peyronie's Disease, as genome-wide studies have reported it: 7 positions from 1 study, the largest recording 3,199 cases and 571,377 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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Urological

Chronic Renal Failure (CKD)

Chronic Renal Failure (CKD), as genome-wide studies have reported it: 2 positions from 1 study, the largest recording 92,642 cases and 521,058 controls (African American or Afro-Caribbean ancestry, Hispanic or Latin American ancestry, East Asian 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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Urological

Nephrotic Syndrome without Mention of Glomerulonephritis

Nephrotic Syndrome without Mention of Glomerulonephritis, as genome-wide studies have reported it: 12 positions from 1 study, the largest recording 1,865 cases and 629,378 controls (African American or Afro-Caribbean ancestry, European 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.

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Urological

Classic Bladder Exstrophy

Classic 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'.

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Urological

Idiopathic Membranous Nephropathy

Idiopathic Membranous Nephropathy, as genome-wide studies have reported it: 4 positions from 1 study, the largest recording 556 cases and 2,338 controls (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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Urological

Benign Prostatic Hyperplasia

A common non-cancerous prostate condition whose genetics barely overlap with prostate cancer's — but that shares enough genetic ground with PSA levels to matter for reading a cancer-screening test correctly.

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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.