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)
Progressive Familial Heart Block
Progressive Microcephaly-seizures-cortical Blindness-developmental Delay Syndrome
Retinitis Pigmentosa 28
Retinitis Pigmentosa 93
Rhabdomyosarcoma
Spherocytosis
Stereotypic Hand Movements
Tp63-related Spectrum Disorders
Type 2hh
Visceral Fat
Waist-to-hip Ratio Adjusted For Bmi X Sex X Age Interaction (4df Test)
3m Syndrome 1
Atrial Fibrillation (phecode 427.21)
Autosomal Dominant Nonsyndromic Hearing Loss 22
Bardet-biedl Syndrome 6
Cholesteryl Esters to Total Lipids Ratio in Large Vldl
Cleft Lip (with or Without Cleft Palate) or Cleft Palate
Coach Syndrome 2
Coronary Artery Calcified Atherosclerotic Plaque (130 Hu Threshold) in Type 2 Diabetes
Crisp3 Protein Levels
Ecg Cardiac Mri Latent Space
Ectopic Tissue
Free Cholesterol Levels in Medium Vldl
Hdl Cholesterol Levels in Current Drinkers
Hypertrophic Cardiomyopathy (mtag)
Il18r1 Protein Levels
Macrocephaly-autism Syndrome
Pelvic Organ Prolapse
Pms2-related Disorder
Postaxial Polydactyly-anterior Pituitary Anomalies-facial Dysmorphism Syndrome
Sgsh Protein Levels
Smoking Behaviour (cigarettes Smoked Per Day)
Sphingomyelin Levels
Stickler Syndrome
Takes Medication For Diabetes/sugar?
X-linked Myopathy with Postural Muscle Atrophy
Alpha Thalassemia
Bilateral Cleft Lip
Cholesterol to Total Lipids in Small Ldl Percentage
Choroideremia
Covid-19 (covid Respiratory Support Vs Population)
Crtac1 Protein Levels
Cst5 Protein Levels
Deficiency of Iodide Peroxidase
Diffuse Cerebral and Cerebellar Atrophy - Intractable Seizures - Progressive Microcephaly Syndrome
Familial Juvenile Hyperuricemic Nephropathy Type 1
Gallstone Disease
Hermansky-pudlak Syndrome 4
Hyperuricemia
Infantile Cortical Hyperostosis
Junctional 5a
Loeys-dietz Syndrome
Lymphedema
Mep1b Protein Levels
Myo7a-related Disorder
Phosphatidylcholine(38:3)_[m+oac]1-/phosphatidylserine(42:2)_[m-h]1- Levels
Phospholipid Levels in Very Large Vldl
Phospholipid Levels in Vldl
Predicted Developmental Stuttering
Premature Atrial Contraction Frequency
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