Health Conditions
52,757 conditions with known genetic associations in our database.
All(52,757)
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)
Congenital Heart Defects
Graves' Disease
Alzheimer's Disease, Proxy Alzheimer's Disease or Related Dementias
Aspartate Aminotransferase to Alanine Aminotransferase Ratio
Autosomal Recessive Nonsyndromic Hearing Loss 9
Developmental Delay
Hereditary Insensitivity to Pain with Anhidrosis
Hereditary Leiomyomatosis and Renal Cell Cancer
Hypogonadotropic Hypogonadism 2 with or Without Anosmia
Noonan Syndrome and Noonan-related Syndrome
Pkd1-related Disorder
Jt Interval
Mitochondrial Complex Iv Deficiency
Polycystic Kidney Disease 2
Selective
Total Lipid Levels in Chylomicrons and Extremely Large Vldl
Hand Grip Strength
Maple Syrup Urine Disease Type 1a
Positive Affect
Type Iii
Cognitive Resilience to Alzheimer's Disease Pathology X Sex Interaction (combined Cognitive Resilience and Educational Attainment Model)
Pmm2-congenital Disorder of Glycosylation
Sex Hormone-binding Globulin Levels and Heel Estimated Bone Mineral Density
Angelman Syndrome
Axonal
Blood Cell Traits Latent Factor 8 (white Cell)
Distal Myopathy with Anterior Tibial Onset
Free Cholesterol to Total Lipids in Large Ldl Percentage
Angelman Syndrome-like
Familial Hemophagocytic Lymphohistiocytosis 3
Adult Hypophosphatasia
Beckwith-wiedemann Syndrome
Concentration of Hdl Particles
Neurodevelopmental Disorder with Hypotonia
Tinnitus
Triglycerides in Small Vldl
Usher Syndrome Type 1b
Cholesteryl Esters to Total Lipids in Large Hdl Percentage
Type 6
Wiedemann-steiner Syndrome
Cholesteryl Esters in Hdl
Greig Cephalopolysyndactyly Syndrome
Polyglandular Autoimmune Syndrome
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2o
Autosomal Recessive Osteopetrosis 1
Basophil Percentage of White Cells
Cholesteryl Ester Levels in Chylomicrons and Extremely Large Vldl
Congenital Myasthenic Syndrome
Glut1 Deficiency Syndrome 1
Granulocyte Percentage of Myeloid White Cells
Hemoglobin A1c (hba1c, Maximum, Inv-norm Transformed)
Inherited Breast Cancer and Ovarian Cancer
Mhc Class Ii Deficiency
Triglycerides to Total Lipids in Very Large Hdl Percentage
Trunk Fat Mass (ukb Data Field 23128)
Cockayne Syndrome Type 2
Familial Thoracic 7
Fanconi Anemia Complementation Group D2
Holocarboxylase Synthetase Deficiency
Type Ib
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