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)
Hayfever
Headache or Hba1c Levels
Hearing Function (2 Khz)
Hereditary Liability to Pressure Palsies
Hereditary Spastic Paraplegia 26
High Altitude Adaptation
Hip Bone Mineral Density and Total Body Fat Mass (bivariate Analysis)
Hippocampal Right Gc-ml-dg Volume (body)
Hnf4a-related Disorder
Hnsha Due to Aldolase A Deficiency
Human Papillomavirus Seropositivity (hpv16 E6/e7/l1)
Hyal1 Protein Levels
Hyperaldosteronism (phecode 255.12)
Hyperphenylalaninemia Due to Dnajc12 Deficiency
Hyperphosphatasia with Intellectual Disability Syndrome 3
Hyperphosphatasia with Intellectual Disability Syndrome 5
Hyperplastic Polyposis Syndrome
Hypertrophic Cardiomyopathy 15
Hypertrophic Obstructive Cardiomyopathy (phecode 425.11)
Hypoplastic Pancreas-intestinal Atresia-hypoplastic Gallbalder Syndrome
Icd10 K44: Diaphragmatic Hernia
Icd10 N81: Female Genital Prolapse
Ichthyosis and Erythrokeratoderma
Ichthyosis Bullosa of Siemens
Idiopathic Central Precocious Puberty
Idua-related Disorder
Ifi30 Protein Levels
Ifnlr1 Protein Levels
Il12b Levels
Il16 Protein Levels
Il17a Levels
Infestation (lice, Mites) (phecode 132)
Influenza A (h1n1) Infection
Insular Cortex Volume
Intellectual Deficiency
Interleukin-1 Receptor Antagonist Protein Levels
Interleukin-1 Receptor-like 2 Levels
Iron (mean, Inv-norm Transformed)
Isolated Microphthalmia 3
Isolated Microphthalmia 8
Itgav Protein Levels
Itgb1bp2/lat2 Protein Level Ratio
Jt Interval (sulfonylurea Treatment Interaction)
Kiaa0586-related Disorder
Kmt2c-related Disorder
Kmt2c-related Ndd
Koebner Type
Lamc2-related Disorder
Lcn15 Protein Levels
Left Ventricular End Diastolic Mass End Diastolic Volume Ratio
Left Ventricular Wall Thickness (maximal)
Lentiform Nucleus Volume
Lethal Congenital Contracture Syndrome 7
Leukocyte Immunoglobulin-like Receptor Subfamily B Member 2 Levels
Leukoencephalopathy with Vanishing White Matter 2
Liddle Syndrome 3
Lonp1-related Disorder
Low Affinity Immunoglobulin Epsilon Fc Receptor Levels
Lrp4-related Disorder
Lymphatic Malformation 7
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