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)
Concentration of Very Small Vldl Particles
Congenital Muscular Hypertrophy-cerebral Syndrome
Eosinophil Percentage of Granulocytes
Hajdu-cheney Syndrome
Juvenile Polyposis/hereditary Hemorrhagic Telangiectasia Syndrome
Naxos Disease
3-methylcrotonyl-coa Carboxylase 2 Deficiency
Amyotrophic Lateral Sclerosis Type 1
Ankyrin-b-related
Baseline Memory X Sex Interaction
Familial Isolated Arrhythmogenic Right Ventricular Dysplasia
Hematocrit (maximum, Inv-norm Transformed)
High Il-1beta Levels in Gingival Crevicular Fluid
Optic Atrophy
Sarcoidosis
Tsc2-related Disorder
Anauxetic Dysplasia
Gut Microbiome Abundance (class Tyzzerella Sp. 3 (at 3 Months) X Any Breastfeeding (3 Months) Interaction
Medication Use (hmg Coa Reductase Inhibitors)
Primary Biliary Cholangitis
Subcortical Volume (mostest)
Succinate-semialdehyde Dehydrogenase Deficiency
Birt-hogg-dube Syndrome 1
Calcium Levels (ukb Data Field 30680)
Endometriosis
Glucose (fasting Status Unknown, Maximum, Inv-norm Transformed)
Life Satisfaction
Lobe Attachment (rater-scored or Self-reported)
Memory Decline in Impaired Cognition X Sex Interaction
Arrhythmogenic Right Ventricular Dysplasia 12
Breast Area Percent Density
Congenital Myopathy with Fiber Type Disproportion
Glucose-6-phosphate Transport Defect
Leg Fat Percentage Left (ukb Data Field 23115)
Autosomal Recessive Nonsyndromic Hearing Loss 1a
Desmin-related Myofibrillar Myopathy
Dupuytren's Disease
Fat-free Mass
Monocyte (absolute Count, Maximum, Inv-norm Transformed)
Neutrophil (absolute Count, Mean, Inv-norm Transformed)
Stickler Syndrome Type 1
Age of Smoking Initiation (mtag)
Carnitine Palmitoyl Transferase 1a Deficiency
Forced Expiratory Volume in 1 Second Fev1 Z Score (ukb Data Field 20256)
Ataxia-telangiectasia-like Disorder
Autosomal
Citrate Levels
Congenital Amegakaryocytic Thrombocytopenia
Pulse Rate (ukb Data Field 102)
Blood Cell Traits Latent Factor 16 (white Cell)
Folate-sensitive
Glycine Encephalopathy 1
Homocystinuria Due to Methylene Tetrahydrofolate Reductase Deficiency
Nijmegen Breakage Syndrome-like Disorder
Retinitis Pigmentosa 80
Triglycerides in Medium Hdl
Achromatopsia 3
Autosomal Dominant 3
Cholesteryl Esters in Medium Hdl
Mps-iii-c
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