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)
Neurodegeneration
Of Pregnancy
Prostate-specific Antigen (psa, Mean, Inv-norm Transformed)
Pyruvate Levels
Tlr3 Protein Levels
Triglyceride Levels in Very Small Vldl
Vertical Cup-disc Ratio (adjusted For Vertical Disc Diameter)
Autosomal Recessive Robinow Syndrome
Average Diameter For Ldl Particles
Basal Ganglia Calcification
Cfhr4 Protein Levels
Cognitive Decline Rate in Late Mild Cognitive Impairment
Fgfr2-related Craniosynostosis
Group D
Idiopathic
Lean Body Mass
Microcephaly 1
Mouth Ulcers
Short Qt Syndrome Type 2
Tctn3 Protein Levels
Alanine Transaminase (alt, Maximum, Inv-norm Transformed)
Aspartate Aminotransferase (ast, Maximum, Inv-norm Transformed)
Autosomal Dominant Nonsyndromic Hearing Loss 12
Autosomal Recessive Nonsyndromic Hearing Loss 18a
Bardet-biedl Syndrome 7
Bicarbonate (mean, Inv-norm Transformed)
Blood Cell Traits Latent Factor 12 (red Cell)
Body Fat Mass
Childhood Ear Infection
Coach Syndrome 3
Cranioectodermal Dysplasia 1
Ectopia Lentis 1
Focal Segmental Glomerulosclerosis
Gut Microbiome Abundance (class Clostridium Sensu Stricto Sp. 17 (at 1 Year) X Any Breastfeeding (3 Months) Interaction
Intellectual Disability-severe Speech Delay-mild Dysmorphism Syndrome
Isoleucine Levels
Kartagener Syndrome
Leber Congenital Amaurosis 5
Mckusick-kaufman Syndrome
Methylmalonic Acidemia with Homocystinuria
Neuroticism Conditioned On Cognitive Performance (multi-trait Conditioning and Joint Analysis)
Putamen Iron Levels (quantitative Susceptibility Mapping)
Timothy Syndrome
Trauma Exposure
Triglyceride Levels in Medium Ldl
Verbal Short Term Memory (paragraph Recall Test)
3-hydroxybutyrate Levels
Abnormal Brain Morphology
Blood Cell Traits Latent Factor 23 (white Cell)
Covid-19 (severe Vs Population)
Cranioectodermal Dysplasia 2
Craniosynostosis Syndrome
Daytime Sleep Phenotypes
Due to 21-hydroxylase Deficiency
Fcrl3 Protein Levels
Fibrochondrogenesis 1
Fibrochondrogenesis 2
Flt4 Protein Levels
Il7r Protein Levels
Maroteaux Type
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