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)
Aseg Global Volume Brainsegnotventsurf
Aseg Global Volume-ratio Brainsegvol-to-etiv
Aseg Lh Intensity Accumbens-area
Aseg Lh Volume Caudate
Aseg Lh Volume Putamen
Aseg Rh Volume Caudate
Aseg Rh Volume Cerebellum-white-matter
Aseg Rh Volume Cerebralwhitematter
Aseg Rh Volume Putamen
Aseg Rh Volume Ventraldc
Asher
Asns-related Disorder
Aspartate--trna Ligase, Mitochondrial Levels
Aspartoacylase Levels
Asphyxia and Hypoxemia (phecode 1013)
Ataxin-3 Levels
Atelis Syndrome 2
Atg4a/nsfl1c Protein Level Ratio
Atn1-related Disorder
Atopy
Atox1/msra Protein Level Ratio
Atp Levels in Blood Donors
Atp Synthase Subunit Beta, Mitochondrial Levels
Atp-dependent Rna Helicase A Levels
Atp-dependent Rna Helicase Dhx8 Levels (dhx8.11601.26.3)
Atp2a2-related Disorder
Atp5if1/lyn Protein Level Ratio
Atp6ap1-related Disorder
Atp6v1g1 Protein Levels
Atr-x-related Syndrome
Atrial Septal Defect 9
Attention Deficit Hyperactivity Disorder or Intracranial Volume (pleiotropy)
Attenuated Familial Adenomatous Polyposis
Autoinflammatory-pancytopenia Syndrome Due to Dnase2 Deficiency
Autosomal Dominant 84
Autosomal Dominant 90
Autosomal Dominant Charcot-marie-tooth Disease Type 2m
Autosomal Dominant Lamellar Ichthyosis
Autosomal Dominant Mendelian Susceptibility to Mycobacterial Diseases Due to Partial Ifngammar1 Deficiency
Autosomal Dominant Nonsyndromic Hearing Loss 41
Autosomal Dominant Nonsyndromic Hearing Loss 51
Autosomal Dominant Nonsyndromic Hearing Loss 68
Autosomal Dominant or Recessive
Autosomal Dominant Vibratory Urticaria
Autosomal Dominant Wooly Hair
Autosomal Erythropoietic Protoporphyria
Autosomal Recessive 109
Autosomal Recessive 121
Autosomal Recessive 33
Autosomal Recessive 60
Autosomal Recessive 63
Autosomal Recessive 64
Autosomal Recessive 67
Autosomal Recessive 94
Autosomal Recessive Cutis Laxa Type 2d
Autosomal Recessive Sensorineural Hearing Loss
Autosomal Recessive Severe Congenital Neutropenia
Avp-related Disorder
Axin1/dapp1 Protein Level Ratio
Axin1/dok2 Protein Level Ratio
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