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)
Chloride Type
Congenital Secretory Diarrhea
Ehlers-danlos Syndrome Due to Tenascin-x Deficiency
Hypertrichotic Osteochondrodysplasia Cantu Type
Il1rl1 Protein Levels
Interleukin-18 Levels
Leopard Syndrome 1
Medication Use For T2d (number of Purchases)
Neutrophil Side Fluorescence
Occupational Income
Phosphatidylethanolamine(36:4)_[m+h]1+ Levels
Phosphatidylethanolamine(38:5)_[m-h]1- Levels
Posterolateral Temporal Area
Primary Erythromelalgia
Stat3 Gain of Function
Transcobalamin Ii Deficiency
With Variable Learning Disabilities and Behavior Disorders
Xeroderma Pigmentosum Group A
Abcb11-related Disorder
Age of Smoking Initiation
Autosomal Recessive 3
Cantagrel Type
Charcot-marie-tooth Disease Type 4f
Cockayne Syndrome Type 1
Covid-19 (covid Pneumonia Vs Population)
Crisp2 Protein Levels
Deficiency of Malonyl-coa Decarboxylase
Developmental Disorder
Femur Total Bone Mineral Density X Gut Microbiota (genus Lactococcus) Interaction
Fetal Akinesia Deformation Sequence 3
Gut Microbial Network Clusters (tan (at 3 Months) X Summer Birth (jun-aug) Interaction
Homocystinuria
Intraocular Pressure (confirmatory Factor Analysis Factor 26)
Klk1 Protein Levels
Leber Congenital Amaurosis 3
Leukoencephalopathy
Neutrophil Side Scatter
Phosphatidylcholine(33:3)_[m+h]1+/phosphatidylethanolamine(36:3)_[m+h]1+/phosphatidate(38:4)_[m+nh4]1+ Levels
Phosphatidylcholine(38:4)_[m+oac]1-/phosphatidylserine(42:3)_[m-h]1- Levels
Pili Torti-deafness Syndrome
Retinitis Pigmentosa 45
Venous Thromboembolism (snp X Snp Interaction)
Wfdc12 Protein Levels
Age At Peak Height Velocity
Autosomal Recessive Limb-girdle Muscular Dystrophy Type R18
Bicarbonate (maximum, Inv-norm Transformed)
Brachyolmia-amelogenesis Imperfecta Syndrome
Carnitine Acylcarnitine Translocase Deficiency
Carpal Tunnel Syndrome
Cholelithiasis
Col2a1 Protein Levels
Dilated Cardiomyopathy 1w
Feeling Worry
Glucose Homeostasis Traits
Klb Protein Levels
Lesch-nyhan Syndrome
Male Infertility with Azoospermia or Oligozoospermia Due to Single Gene Mutation
Methylmalonic Aciduria and Homocystinuria Type Cbld
Microangiopathy and Leukoencephalopathy
Noonan Syndrome 10
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