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)
3 Beta-hydroxysteroid Dehydrogenase Deficiency
Acquired
Acute Recurrent
Adam22 Protein Levels
Adam23 Protein Levels
Alpha-fetoprotein Levels
Amy2a Protein Levels
And Tooth Agenesis
Apol1 Protein Levels
Autosomal Dominant 22
Autosomal Recessive Nonsyndromic Hearing Loss 31
C7 Protein Levels
Cdh6 Protein Levels
Cerebral Palsy
Charcot-marie-tooth Disease Axonal Type 2k
Childhood Aggressive Behavior
Cholesteryl Esters in Very Large Hdl (ukb Data Field 23555)
Chondrodysplasia Punctata 2 X-linked Dominant
Cntn2 Protein Levels
Coffin-siris Syndrome 6
Cognitive Function (immediate Memory) (longitudinal)
Combined Psap Deficiency
Concentration of Medium Hdl Particles (ukb Data Field 23565)
Cone Dystrophy
Congenital Glucose-galactose Malabsorption
Cornelia De Lange Syndrome 4
Corpus Callosum Mid Anterior Subregion Volume
Corpus Callosum Splenium Area
Cpq Protein Levels
Crygd Protein Levels
Cubn-related Disorder
Dhcr7-related Disorder
Familial Adult Myoclonic
Gfral Protein Levels
Global Cognition (mini Mental State Examination)
Glutathione Synthetase Deficiency with 5-oxoprolinuria
Gut Microbial Network Clusters (turquoise (at 3 Months) X Spring Birth (mar-may) Interaction
Haddad Syndrome
Hepatitis B
Hereditary Diffuse Leukoencephalopathy with Spheroids
Hermansky-pudlak Syndrome 5
Hypertrophic Cardiomyopathy 12
Infantile Onset Spinocerebellar Ataxia
Insomnia Symptoms (never/rarely Vs. Sometimes/usually)
Intellectual Developmental Disorder with Dysmorphic Facies and Ptosis
Interleukin-10 Levels
Keratoderma
Kir2dl2 Protein Levels
Lair2 Protein Levels
Marinesco-sjögren Syndrome
Methylmalonic Aciduria and Homocystinuria Type Cblf
Microalbuminuria
Monobrow
Myhre Syndrome
Neuritic Plaque
Neurodegeneration with Ataxia and Late-onset Optic Atrophy
Nonsyndromic Orofacial Clefts
Oligosynaptic Infertility
Optic Disc Area
Pex1-related Disorder
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