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)
Global Developmental Delay
Primary Hyperoxaluria
Dna Methylation Variation (age Effect)
Eosinophill Percentage (ukb Data Field 30210)
Hereditary Spastic Paraplegia 4
Pulmonary Fibrosis And/or Bone Marrow Failure
Breast Dense Area
Type 1 Diabetes
Triglyceride to Hdl Cholesterol Ratio
Bipolar Disorder
Usher Syndrome Type 1d
Autosomal Dominant Alport Syndrome
Autosomal Recessive Nonsyndromic Hearing Loss 2
Fev1
Platelet Count (mean, Inv-norm Transformed)
Igf 1 (ukb Data Field 30770)
Type 2c
With Axonal Neuropathy 2
Von Hippel-lindau Syndrome
Low-density Lipoprotein Levels
Asthma (childhood Onset)
Oligodontia-cancer Predisposition Syndrome
Autosomal Dominant 5
Glycated Haemoglobin Hba1c Levels (ukb Data Field 30750)
Igg Glycosylation
Lymphangiomyomatosis
Arrhythmogenic Right Ventricular Dysplasia 9
Alport Syndrome
Neurofibromatosis-noonan Syndrome
Saturated Fatty Acids to Total Fatty Acids Percentage
Autism Spectrum Disorder
Mucolipidosis Type Ii
Cystatin C Levels
Dystrophin Deficiency
Idiopathic Pulmonary Fibrosis
Zellweger Spectrum Disorders
Personality Traits or Cognitive Traits (multivariate Analysis)
Severe Combined Immunodeficiency
Amyotrophic Lateral Sclerosis Type 4
B Cell-negative
Glaucoma
Autosomal Recessive Nonsyndromic Hearing Loss 4
Electrocardiogram Morphology (amplitude At Temporal Datapoints)
What Is Your Height? (cm, Inv-normal Transformed)
Autosomal Dominant 1
Non-albumin Protein Levels
T Cell-negative
Estimated Glomerular Filtration Rate Based On Creatinine and Cystatin C in Bottom 99% of Individuals By Creatinine Levels
Autosomal Recessive Limb-girdle Muscular Dystrophy
High Light Scatter Reticulocyte Percentage (ukb Data Field 30290)
Impedance of Whole Body (ukb Data Field 23106)
Dilated Cardiomyopathy 1dd
Landau-kleffner Syndrome
Fetal Akinesia Deformation Sequence 1
Junctional Epidermolysis Bullosa Gravis of Herlitz
Congenital Hyperammonemia
Ovarian Neoplasm
Café-au-lait Macules with Pulmonary Stenosis
Lymphocyte Count (ukb Data Field 30120)
Norman-roberts Syndrome
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