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)
Paralemmin-1 Levels
Paramyotonia Congenita/hyperkalemic Periodic Paralysis
Paraneoplastic Antigen Ma2 Levels
Paraoxonase Levels
Parent of Origin Effect On Language Impairment (paternal)
Park7/txnrd1 Protein Level Ratio
Paroxysmal Central Nervous System Disorders
Parp1 Protein Levels
Patatin-like Phospholipase Domain-containing Protein 2 Levels
Patent Ductus Arteriosus 2
Pathological, Developmental or Recurrent Dislocation (phecode 742.2)
Paul-chao Neurodevelopmental Syndrome
Pca3 Expression Level
Pcbp2 Protein Levels
Pcyt2 Protein Levels
Pdcd1/tnfrsf4 Protein Level Ratio
Pdcd1/tnfrsf8 Protein Level Ratio
Pdgfb/sparc Protein Level Ratio
Pdhx-related Disorder
Pdlim5 Protein Levels
Pdlim7/ppp1r9b Protein Level Ratio
Pdlim7/tbc1d23 Protein Level Ratio
Pdx1-related Disorder
Pdz and Lim Domain Protein 4 Levels
Pdzd2 Protein Levels
Peanut Allergy (maternal Genetic Effects)
Peho-like Syndrome
Peptidyl-prolyl Cis-trans Isomerase D Levels
Peptidyl-prolyl Cis-trans Isomerase Fkbp4 Levels
Peptidyl-prolyl Cis-trans Isomerase G Levels
Percentage of Core-fucosylation of Trigalactosylated Structures (gp111)
Percentage of Fa2g1 in Total Neutral Plasma Glycans (gpn) (gp61)
Percentage of Fa2g2 in Total Neutral Plasma Glycans (gpn) (gp67)
Pericardial Fat (model 2)
Peripheral or Central Vertigo (phecode 386.2)
Periventricular Nodular Heterotopia 6
Periventricular Nodular Heterotopia with Syndactyly
Permanent Tooth Development
Peroxisomal 2,4-dienoyl-coa Reductase Levels
Persistent Truncus Arteriosus
Persulfide Dioxygenase Ethe1, Mitochondrial Levels
Pes Planus
Pfkfb2/serpinb1 Protein Level Ratio
Pgm3-related Disorder
Phenylacetate Levels
Phenylalanine Levels (ukb Data Field 23468)
Philadelphia Chromosome-positive
Phka2-related Disorder
Phkg2-related Disorder
Phonological Awareness (elision)
Phosphatidylcholine (16:0_16:1) Levels
Phosphatidylcholine (16:0_20:3) (b) Levels
Phosphatidylcholine (16:1_18:0) Levels
Phosphatidylcholine (18:0_20:2) Levels
Phosphatidylcholine (18:0_22:4) Levels
Phosphatidylcholine (38:4) (b) Levels
Phosphatidylcholine (o-16:0_18:2) Levels
Phosphatidylcholine (o-16:1_18:1) Levels
Phosphatidylcholine (o-16:2_18:0) Levels
Phosphatidylcholine (o-18:1_18:2) Levels
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