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)
Retinitis Pigmentosa 38
Serum Total Triglyceride Levels
Siops Occupational Score
Spondylocarpotarsal Synostosis Syndrome
Ssc5d Protein Levels
Trimethylaminuria
Vaginal Microbiome Metacyc Pathway (meth-acetate-pwy|methanogenesis From Acetate)
Acetone Levels
Autosomal Dominant Nonsyndromic Hearing Loss 36
Bartter Disease Type 3
Body Mass Index in Cystic Fibrosis
Brown-vialetto-van Laere Syndrome 2
Cd48 Protein Levels
Cerebellar Atrophy
Chloride (minimum, Inv-norm Transformed)
Cholesteryl Esters in Medium Hdl (ukb Data Field 23569)
Christianson Syndrome
Chronic Rhinosinusitis with Nasal Polyposis
Complementation Group K
Congenital Dyserythropoietic
Congenital Myasthenic Syndrome 2a
Dheas Levels
Disruptive Behavior (multivariate Analysis)
Edar Protein Levels
Familial Horizontal
Folr3 Protein Levels
Gal Protein Levels
Gaze Palsy
Ghrelin Levels
Hemochromatosis Type 4
Hereditary Motor and Sensory
Hermansky-pudlak Syndrome 6
Hip Minimal Joint Space Width
Human Milk Oligosaccharide Concentration (2'-fucosyllactose)
Immunodeficiency-centromeric Instability-facial Anomalies Syndrome 1
Iron Status Biomarkers (ferritin Levels)
Loeys-dietz Syndrome 1
Maximum Habitual Alcohol Consumption
Muscular Dystrophy-dystroglycanopathy Type B5
Myoglobinuria
Nicotine Dependence and Major Depression (severity of Comorbidity)
Nonsyndromic Orofacial Cleft X Sex Interaction
Pah-related Disorder
Partial Hypoxanthine-guanine Phosphoribosyltransferase Deficiency
Phosphatidylcholine(40:6)_[m+h]1+/phosphatidylethanolamine(43:6)_[m+h]1+ Levels
Pierpont Syndrome
Premature Ovarian Failure
Rapadilino Syndrome
Saturated Fatty Acid Percentage of Total Fatty Acids
Seropositivity For Streptococcus Pyogenes Peptide (agilent_220658)
Severe Combined Immunodeficiency Due to Dna-pkcs Deficiency
Short Stature-optic Atrophy-pelger-huët Anomaly Syndrome
Suicide Attempts
Tor1aip1 Protein Levels
Type 5a
Type A14
Tyrosine Kinase Inhibitor Response
Waardenburg Syndrome Type 2e
Wfikkn2 Protein Levels
X-linked 19
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