Conditions

Continuously updated · last reviewed Sep 5, 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. 27 conditions so far, growing continuously, and free to reuse with attribution (CC BY 4.0).

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All 27 Autoimmune 1 Cardiovascular 2 Dermatologic 2 Hematologic 3 Immunologic 3 Metabolic 5 Neurological 2 Nutritional 1 Ophthalmic 1 Pharmacogenomics 4 Sensory 3

3 results in Hematologic

Hematologic

ABO Blood Group

The ABO gene variant that creates blood type O by disabling its enzyme, why blood type matters for transfusion, and which disease links (clotting risk, malaria, cholera) are strong versus which (COVID-19, cancer risk) remain modest or contested.

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Hematologic

Duffy-Null Phenotype and Benign Ethnic Neutropenia

A promoter variant that silences the Duffy antigen on red cells, protecting against Plasmodium vivax malaria and causing a normal, lower neutrophil count that is routinely and wrongly treated as disease in people of African ancestry.

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Hematologic

Factor V Leiden Thrombophilia

A common inherited change in the F5 gene that makes blood slightly slower to switch off clotting, raising the risk of deep vein thrombosis and pulmonary embolism. Most carriers never have a clot.

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