Health Conditions

43,676 conditions with known genetic associations in our database.

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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)
Heel Bone Mineral Density X Serum Urate Levels Interaction
159 variants Other
Joubert Syndrome 3
159 variants Other
Medication Use (diuretics)
159 variants Other
Myeloid White Cell Count
159 variants Other
Sex Hormone-binding Globulin Levels in Postmenopausal Women
159 variants Other
Basophil (fraction, Mean, Inv-norm Transformed)
158 variants Other
Biological Sex
158 variants Other
Concentration of Idl Particles
158 variants Other
Familial Multiple Polyposis Syndrome
158 variants Other
Kufor-rakeb Syndrome
158 variants Other
Adult-onset
157 variants Other
Autosomal Recessive Spastic Paraplegia Type 78
157 variants Other
Charcot-marie-tooth Disease Type 4c
157 variants Other
Cone-rod Dystrophy 6
157 variants Other
Depressed Affect
157 variants Other
Glycogen Storage Disease Due to Glucose-6-phosphatase Deficiency Type Ia
157 variants Other
Hereditary Factor Xi Deficiency Disease
157 variants Other
Iodotyrosyl Coupling Defect
157 variants Other
Lethal Kniest-like Syndrome
157 variants Other
Neutrophil (fraction, Mean, Inv-norm Transformed)
157 variants Other
Neutrophil (fraction, Minimum, Inv-norm Transformed)
157 variants Other
Peripheral Arterial Disease (traffic-related Air Pollution Interaction)
157 variants Other
Red Blood Cell Count (rbc, Minimum, Inv-norm Transformed)
157 variants Other
Triglyceride (mean, Inv-norm Transformed)
157 variants Other
Vps13b-related Disorder
157 variants Other
Actin Accumulation Myopathy
156 variants Other
Combined Immunodeficiency Due to Lrba Deficiency
156 variants Other
Congenital Disorder of Glycosylation
156 variants Other
Proteinuria
156 variants Other
Waist Circumference (ukb Data Field 48)
156 variants Other
Cep290-related Disorder
155 variants Other
Corneal Dystrophy
155 variants Other
Pfeiffer Syndrome
155 variants Other
Hematocrit (mean, Inv-norm Transformed)
154 variants Other
Hypomyelinating
154 variants Other
Osteogenesis Imperfecta Type 8
154 variants Other
Permanent Neonatal 3
154 variants Other
Pitt-hopkins-like Syndrome 2
154 variants Other
Cerebellar Ataxia
153 variants Other
Lipoprotein A Levels (ukb Data Field 30790)
153 variants Other
Urinary Albumin-to-creatinine Ratio
153 variants Other
Blood Urea Nitrogen (bun, Mean, Inv-norm Transformed)
152 variants Other
Chorea-acanthocytosis
152 variants Other
Fasting Plasma Glucose
152 variants Other
Fumarase Deficiency
151 variants Other
Infantile Gm1 Gangliosidosis
151 variants Other
Noncognitive Aspects of Educational Attainment
151 variants Other
Triglyceride (maximum, Inv-norm Transformed)
151 variants Other
Dystonia 12
150 variants Other
Familial Hemophagocytic Lymphohistiocytosis 2
150 variants Other
Familial Hypocalciuric Hypercalcemia 1
150 variants Other
Granulocyte Count
150 variants Other
Joubert Syndrome 7
150 variants Other
Lymphocyte (fraction, Maximum, Inv-norm Transformed)
150 variants Other
Monocytopenia with Susceptibility to Infections
150 variants Other
Valine Levels
150 variants Other
Von Willebrand Disease Type 3
150 variants Other
Waist-to-hip Ratio Adjusted For Body Mass Index
150 variants Other
And Developmental Delay
149 variants Other
Cdkl5 Disorder
149 variants Other
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