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)
Sulfite Oxidase Deficiency
Symmetrical Dyschromatosis of Extremities
Syndromic X-linked Intellectual Disability Najm Type
6-month Creatinine Clearance Change Response to Tenofovir Treatment in Hiv Infection (treatment Arm Interaction)
Anophthalmia-microphthalmia Syndrome
Ascending Aorta Maximum Area
Autosomal Recessive Ataxia Due to Ubiquinone Deficiency
Fbn1-related Disorder
Femoral Neck Bone Mineral Density
Hematocrit (minimum, Inv-norm Transformed)
Papillon-lefèvre Syndrome
Phosphatidylcholine(38:3)_[m+h]1+/phosphatidylethanolamine(41:3)_[m+h]1+/phosphatidate(43:4)_[m+nh4]1+ Levels
Piezo1-related Disorder
Response to Amphetamines
Somatic
Trail Levels
Triglyceride Levels in Small Hdl
1,5-anhydroglucitol (1,5-ag) Levels
3m Syndrome 2
Alg9 Congenital Disorder of Glycosylation
Bilirubin Levels
Coffin-lowry Syndrome
Complement Component 3 Deficiency
Congenital Microvillous Atrophy
Cpvl Protein Levels
Developmental and Epileptic Encephalopathy 6b
Elevated Prostate Specific Antigen [psa] (phecode 796)
Gracile Syndrome
Hereditary Mixed
Hypercalcemia
Leber Congenital Amaurosis 4
Major Depressive Disorder (mtag)
Mbl2 Protein Levels
Msmb Protein Levels
Polyposis Syndrome
Retinitis Pigmentosa 4
Spastic Ataxia
Triglyceride Levels in Idl
Velopharyngeal Dysfunction
Acromesomelic Dysplasia 1
Age At First Birth
Autosomal Dominant Nonsyndromic Hearing Loss 1
Autosomal Recessive Nonsyndromic Hearing Loss 21
Bilateral Frontoparietal Polymicrogyria
Cenani-lenz Syndactyly Syndrome
Cerebral Creatine Deficiency Syndrome
Col2a1-related Disorder
Cowden Syndrome
Dkkl1 Protein Levels
F12 Protein Levels
Fish- and Plant-related Diet
Gaucher Disease Type I
Majeed Syndrome
Noonan Syndrome 2
Occipital Area
Pdcd1lg2 Protein Levels
Peroxisome Biogenesis Disorder 5a (zellweger)
Peroxisome Biogenesis Disorder 6a (zellweger)
Photosensitive
Sunburns
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