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)
Human Milk Oligosaccharide Concentration (sialyl-lacto-n-tetraose C)
Huntington Disease-like 1
Hypohidrosis-enamel Hypoplasia-palmoplantar Keratoderma-intellectual Disability Syndrome
Icd10 J35: Chronic Diseases of Tonsils and Adenoids
Idiopathic Fibrosing Alveolitis (phecode 504.1)
Igfbp7 Protein Levels
Imerslund-grasbeck Syndrome Type 2
Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Type 1
Infantile Spasms
Infertility Disorder
Inflammatory or Infectious Upper Respiratory Disease
Inherited Prostate Cancer
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or Without Seizures
Interleukin-5 Levels
Invasive Melanoma
Iron-refractory Iron Deficiency Anemia
Isolated Microphthalmia 6
Kcnh2-related Disorder
Kcnt1-related Disorder
Keratoconus 1
Keratosis Follicularis
Kif5a-related Disorder
Klk10 Protein Levels
Klk7 Protein Levels
L1cam-related Disorder
Lad1 Protein Levels
Late-onset Alzheimer's Disease (adjusted For Apoe)
Left Eye Overall Retinal Pigment Epithelium Thickness
Lethal Congenital Contracture Syndrome 11
Lethal Left Ventricular Non-compaction-seizures-hypotonia-cataract-developmental Delay Syndrome
Lifetime Major Depressive Disorder (autocomplete Impute)
Lipoprotein-associated Phospholipase A2 Activity and Mass
Lisch Epithelial Corneal Dystrophy
Loneliness (multivariate Analysis)
Ltbp2 Protein Levels
Malignant Neoplasm of Bladder (phecode 189.21)
Maturity-onset Diabetes of the Young Type 4
Mcp1 Levels
Mdk Protein Levels
Megalencephaly-polymicrogyria-postaxial Polydactyly-hydrocephalus Syndrome
Mendelian Susceptibility to Mycobacterial Diseases Due to Complete Il12b Deficiency
Meningioma
Microspherophakia And/or Megalocornea
Migraine or Glucose Levels
Miller Syndrome
Mitochondrial Dna Heteroplasmy (chrm:302:a:ac Case-only Heteroplasmy)
Monogenic Short Statue
Multiple Epiphyseal Dysplasia Type 5
Multiple Self-healing Squamous Epithelioma
Multisystem Inflammatory Syndrome in Children
N-acetyl-aspartyl-glutamate (naag) Levels in Elite Athletes
N-acetylcarnosine Levels
N-acylethanolamine-hydrolyzing Acid Amidase Levels
Nail-patella-like Renal Disease
Ncan Protein Levels
Neonatal Hypotonia
Nephronophthisis 14
Neuroendocrine Tumors (phecode 209)
Neutrophil Side Fluorescence Distribution Width
Nicotine Metabolite Ratio in Current Smokers
Upload your DNA to discover which genetic variants you carry and assess your risk.
Get Started Free →