Health Conditions

43,676 conditions with known genetic associations in our database.

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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)
High-density Lipoprotein Levels
643 variants Other
Type C1
637 variants Other
High-density Lipoprotein Levels (mtag)
632 variants Other
Juvenile Polyposis Syndrome
630 variants Other
Calcium Levels
626 variants Other
Muscular Dystrophy
620 variants Other
Muscular Dystrophy-dystroglycanopathy (congenital with Intellectual Disability)
620 variants Other
Becker Muscular Dystrophy
617 variants Other
Neurodevelopmental Disorder
617 variants Other
Hereditary Hemorrhagic
615 variants Other
Neuronal Ceroid Lipofuscinosis
615 variants Other
Telangiectasia
615 variants Other
Severe Covid-19 Infection
614 variants Other
Glycine Encephalopathy
611 variants Other
Serum Metabolite Levels
603 variants Other
Lymphocyte Percentage of White Cells
599 variants Other
Mitochondrial Complex I Deficiency
595 variants Other
Triglyceride Levels (mtag)
595 variants Other
Normal Intelligence and Immunodeficiency
593 variants Other
Cognitive Performance (mtag)
592 variants Other
X-linked Dominant
591 variants Other
Heterotopia
590 variants Other
Vertex-wise Cortical Thickness
589 variants Other
Periventricular
588 variants Other
Mean Corpuscular Haemoglobin (ukb Data Field 30050)
587 variants Other
Episodic Ataxia Type 2
586 variants Other
Externalizing Behaviour (multivariate Analysis)
579 variants Other
Prostate-specific Antigen Levels
579 variants Other
Autosomal Recessive Limb-girdle Muscular Dystrophy Type 2b
575 variants Other
Femur Bone Mineral Density X Serum Urate Levels Interaction
573 variants Other
Serum Total Protein Levels
568 variants Other
Primary Familial Hypertrophic Cardiomyopathy
567 variants Other
Cftr-related Disorder
564 variants Other
Hereditary Spastic Paraplegia 11
560 variants Other
Menarche (age At Onset)
560 variants Other
Cornelia De Lange Syndrome 1
559 variants Other
Glycogen Storage Disease Type Iii
559 variants Other
Limb-girdle
559 variants Other
Memory Decline in Normal Cognition
559 variants Other
Isolated Focal Cortical Dysplasia Type Ii
558 variants Other
Li-fraumeni Syndrome 1
558 variants Other
Neutrophil Percentage of White Cells
558 variants Other
Retinitis Pigmentosa 25
557 variants Other
Curry-hall Syndrome
555 variants Other
Adult Body Size
554 variants Other
Arthrogryposis Multiplex Congenita 6
553 variants Other
Body Fat Percentage (adjusted For Testosterone and Shbg)
551 variants Other
Mean Corpuscular Volume (ukb Data Field 30040)
550 variants Other
Body Size (confirmatory Factor Analysis Factor 21)
549 variants Other
Vertical Cup-disc Ratio
547 variants Other
Oto-palato-digital Syndrome
545 variants Other
Peroxisome Biogenesis Disorder
544 variants Other
Self-reported Math Ability
544 variants Other
Propionic Acidemia
543 variants Other
Melnick-needles Syndrome
541 variants Other
Frontometaphyseal Dysplasia
540 variants Other
Hypokalemic Periodic Paralysis
540 variants Other
Memory Decline
539 variants Other
Height (mean, Inv-normal Transformed)
537 variants Other
Neuroblastoma
537 variants Other
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