Health Conditions
43,676 conditions with known genetic associations in our database.
All(43,676)
Other(43,676)
Cardiovascular(1,793)
Metabolic(1,614)
Renal(1,319)
Cancer(1,257)
Neurological(750)
Ophthalmic(535)
Gastrointestinal(367)
Hematologic(345)
Respiratory(323)
Autoimmune(265)
Dermatologic(221)
Pharmacogenomic(163)
Musculoskeletal(129)
Right Hippocampal Volume
Sphingomyelin(42:3)_[m+h]1+ Levels
Symbol Digit Substitution Test Performance (baseline)
Tea Consumption
Type 11
Umod Protein Levels
Vascular Endothelial Growth Factor Levels
Apc-associated Polyposis Disorders
Apob-related Disorder
Autosomal Recessive Nonsyndromic Hearing Loss 30
Cholelithiasis (ukb Data Field 20002_1162)
Developmental Delay with Variable Intellectual Impairment and Behavioral Abnormalities
Dystonia 28
Early Myoclonic Encephalopathy
Gut Microbiome Abundance (class Anaerostipes Sp. (at 3 Months) X Any Breastfeeding (3 Months) Interaction
Immunodeficiency 31b
Impaired Speech
Lactate Levels
Leukoencephalopathy with Brain Stem and Spinal Cord Involvement-high Lactate Syndrome
Lumbar Spine Bone Mineral Density
Malan Overgrowth Syndrome
Mandibular Hypoplasia-deafness-progeroid Syndrome
Mean Diameter of Hdl Particles
Mitochondrial Complex Iii Deficiency Nuclear Type 1
Optic Cup Area
Prss27 Protein Levels
Saturated Fatty Acid Levels
Shmt1 Protein Levels
Substantia Nigra Iron Levels (quantitative Susceptibility Mapping)
Tenofovir Clearance in Hiv Infection
Tnf Receptor-associated Periodic Fever Syndrome (traps)
Tremor
Triglyceride Levels X Alcohol Consumption (regular Vs Non-regular Drinkers) Interaction (2df)
Alcohol Use Frequency in Early Adulthood
Autosomal Recessive Nonsyndromic Hearing Loss 7
Cask-related
Cbl-related Disorder
Ccl25 Protein Levels
Cholesteryl Esters in Medium Vldl
Combined Oxidative Phosphorylation Defect Type 14
Dnah5-related Disorder
Duane-radial Ray Syndrome
Ep300-related Disorder
Farber Lipogranulomatosis
Feeling Nervous
Femoral Neck Width
Gut Microbiota (bacterial Taxa)
Hereditary Spastic Paraplegia 10
Hereditary Xanthinuria Type 1
Hypogonadotropic Hypogonadism 1 with or Without Anosmia
Ifngr2 Protein Levels
Irritable Mood
Left Hippocampal Volume
Long Qt Syndrome 8
Methylmalonic Aciduria Due to Complete Methylmalonyl-coa Mutase Deficiency
Mosaic Loss of Chromosome Y (y Chromosome Dosage)
Moyamoya Disease
Nuclear Type 16
Oculocutaneous Albinism Type 4
Parental Longevity (mother's Age At Death)
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