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)
Lama3-related Disorder
Lamb Consumption
Language Functional Connectivity
Lepr-related Disorder
Lethal Osteosclerotic Bone Dysplasia
Lifr Levels
Linoleic Acid to Total Fatty Acids Percentage (ukb Data Field 23456)
Lipa-related Disorder
Lipase Deficiency
Loneliness (linear Analysis)
Long Qt Syndrome 10
Male Puberty Timing (early Vs. Average Onset Voice Breaking)
Martsolf Syndrome 1
Medial Orbital Frontal Cortex Volume
Megf9 Protein Levels
Microcephaly-capillary Malformation Syndrome
Mitf-related Disorder
Moderate Global Developmental Delay
Mthfsd Protein Levels
Mutilating Keratoderma
Myo18b-related Disorder
N-acetylphenylalanine Levels
N1-methyl-2-pyridone-5-carboxamide Levels
Neurofibroma
Nicotine Withdrawal
Noonan Syndrome-like Disorder with Loose Anagen Hair 1
Occlusion and Stenosis of Precerebral Arteries (phecode 433.1)
Oligodontia
Osteogenesis Imperfecta Type 10
Osteogenesis Imperfecta Type 15
Other Hypertrophic Cardiomyopathy (phecode 425.12)
P Wave Duration
Paget Disease of Bone 3
Pain
Palmitoyl Dihydrosphingomyelin (d18:0/16:0) Levels
Pappalysin-1 Levels
Pdl1 Levels
Peroxisome Biogenesis Disorder 8a (zellweger)
Phosphatidylcholine (15:0_20:4) Levels
Phosphatidylcholine_34:0_[m+h]1+/phosphatidylethanolamine_37:0_[m+h]1+/phosphatidate_39:1_[m+nh4]1+ Levels
Phosphatidylinositol (18:0_18:2) Levels
Phosphatidylinositol(34:1)_[m-h]1- Levels
Phosphatidylinositol(35:2)_[m-h]1- Levels
Phosphatidylinositol(40:5)_[m-h]1- Levels
Pi16 Protein Levels
Pklr-related Disorder
Plasma Factor V Levels (parent of Origin Effect) X Rs75463553 Interaction
Plasma Omega-3 Polyunsaturated Fatty Acid Levels (alphalinolenic Acid)
Pontocerebellar Hypoplasia Type 5
Ppy Protein Levels
Preeclampsia (maternal Genotype Effect)
Primary Failure of Tooth Eruption
Programmed Cell Death 1 Ligand 2 Levels
Prothrombin Time
Psat Deficiency
Psoriatic Arthropathy (phecode 696.42)
Purpura and Other Hemorrhagic Conditions (phecode 287)
Pygm-related Disorder
Rbm20-related Disorder
Regional Cortical Thickness (inferiorparietal)
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