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)
Steel Syndrome
Stx7 Protein Levels
Symptomatic Extra- and Intra-cranial Atherosclerotic Stenosis
Syndromic X-linked Intellectual Disability 94
Tcirg1-related Disorder
Tfpi2 Protein Levels
Total Body Bone Mineral Density (mtag)
Transient Bullous Dermolysis of the Newborn
Trigonocephaly 2
Tryptase Beta-2 Levels
Tuberculosis (snp X Snp Interaction)
Type Iii Caused By Mutation in Prkcd
Usher Syndrome Type 3
Vaginal Microbiome Relative Abundance (o_fusobacteriales)
Venous Thromboembolism or Factor Vii Levels (pleiotropy)
Venous Thromboembolism or Factor Viii Levels (pleiotropy)
Wdr35-related Disorder
With Vocal Cord Paresis
X-24309 Levels
X-linked 3
1,2-dilinoleoyl-gpc (18:2/18:2) Levels
2-hydroxyphenylacetate Levels
Abcg5-related Disorder
Academic Attainment (science)
Alanine Levels (ukb Data Field 23460)
Alkalosis Syndrome
Alpha-aminoadipic Acid Levels
And Skeletal Defects with or Without Seizures
Anxa2 Protein Levels
Arthrogryposis Multiplex Congenita 3
Atrn Protein Levels
Autosomal Dominant 46
Autosomal Dominant 51
Autosomal Recessive Osteopetrosis 7
Autosomal Recessive Spastic Paraplegia Type 76
Basophil Percentage of White Cells Variance
Birth Length (mtag)
Bitter Beverage Consumption
Body Mass Index in Physically Inactive Individuals
Ca12 Protein Levels
Ca4 Protein Levels
Ccl23 Protein Levels
Cerebellar Ataxia-areflexia-pes Cavus-optic Atrophy-sensorineural Hearing Loss Syndrome
Charcot-marie-tooth Disease Type 4b3
Cheese Consumption
Childhood Gender Nonconformity
Cholesteryl Ester_22:6_[m+nh4]1+ Levels
Chopra-amiel-gordon Syndrome
Cleft Lip/palate-ectodermal Dysplasia Syndrome
Coeliac Disease
Cog4-congenital Disorder of Glycosylation
Combined Oxidative Phosphorylation Defect Type 27
Complement C4 Levels (c4a.c4b.4481.34.2)
Cone-rod Dystrophy 9
Congenital Aneurysm of Ascending Aorta
Congenital Disorder of Deglycosylation 1
Corpus Callosum Genu Area
Corpus Callosum Isthmus Area
Cortical Dysplasia
Coxopodopatellar Syndrome
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