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)
Muscular Dystrophy-dystroglycanopathy Type B5
Myoglobinuria
Nicotine Dependence and Major Depression (severity of Comorbidity)
Nonsyndromic Orofacial Cleft X Sex Interaction
Pah-related Disorder
Parkinsonian-pyramidal Syndrome
Partial Hypoxanthine-guanine Phosphoribosyltransferase Deficiency
Phosphatidylcholine(40:6)_[m+h]1+/phosphatidylethanolamine(43:6)_[m+h]1+ Levels
Pierpont Syndrome
Platelet-type Bleeding Disorder 10
Premature Ovarian Failure
Pseudohypoparathyroidism Type I A
Rapadilino Syndrome
Renal Disease 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
Total Cholesterol to Total Lipids Ratio in Small Ldl
Type 5a
Type A14
Tyrosine Kinase Inhibitor Response
Waardenburg Syndrome Type 2e
Wfikkn2 Protein Levels
X-linked 19
3 Beta-hydroxysteroid Dehydrogenase Deficiency
Acquired
Acute Recurrent
Adam22 Protein Levels
Adam23 Protein Levels
Alpha-fetoprotein Levels
Amy2a Protein Levels
And Tooth Agenesis
Apol1 Protein Levels
Autosomal Dominant 22
Autosomal Recessive Nonsyndromic Hearing Loss 31
Barrett's Esophagus or Esophageal Adenocarcinoma
C7 Protein Levels
Cdh6 Protein Levels
Cerebral Palsy
Charcot-marie-tooth Disease Axonal Type 2k
Childhood Aggressive Behavior
Cholesterol Esters in Medium Vldl
Cholesterol in Medium Hdl (ukb Data Field 23568)
Cholesteryl Esters in Very Large Hdl (ukb Data Field 23555)
Chondrodysplasia Punctata 2 X-linked Dominant
Cntn2 Protein Levels
Coffin-siris Syndrome 6
Cognitive Function (immediate Memory) (longitudinal)
Combined Psap Deficiency
Concentration of Medium Hdl Particles (ukb Data Field 23565)
Cone Dystrophy
Congenital Glucose-galactose Malabsorption
Cornelia De Lange Syndrome 4
Corpus Callosum Mid Anterior Subregion Volume
Corpus Callosum Splenium Area
Cpq Protein Levels
Crygd Protein Levels
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