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)
Gut Microbiome Abundance (class Clostridium Sensu Stricto Sp. (at 3 Months) X Spring Birth (mar-may) Interaction
Gut Microbiome Abundance (class Clostridium Sensu Stricto Sp. 17 (at 1 Year) X Vaginal Birth Interaction
Gzmh Protein Levels
H3 K27-altered
Head Width to Trunk Length Ratio
Hearing Function
Hereditary Spastic Paraplegia 43
Hiv Setpoint Viral Load
Human Milk Oligosaccharide Concentration (sialyl-lacto-n-tetraose C)
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
Infantile Spasms
Infertility Disorder
Intellectual Developmental Disorder with Behavioral Abnormalities and Craniofacial Dysmorphism with or Without Seizures
Interleukin-5 Levels
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
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
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
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
Ncan Protein Levels
Neonatal Hypotonia
Neutrophil Side Fluorescence Distribution Width
Nicotine Metabolite Ratio in Current Smokers
Nontoxic Multinodular Goiter (phecode 241.2)
Notch2 Protein Levels
Nrxn1-related Disorder
Opg Levels
Parental Lifespan
Pccb-related Disorder
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