Health Conditions

52,757 conditions with known genetic associations in our database.

All(52,757) 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)
Hypomyelinating Leukodystrophy 9
15 variants Other
Hypoplastic Left Heart Syndrome 1
15 variants Cardiovascular
Idiopathic Downbeat Nystagmus
15 variants Other
Idiopathic Intracranial Hypertension
15 variants Cardiovascular
Ifih1-related Disorder
15 variants Other
Impaired Intellectual Development
15 variants Other
Inattentive Symptoms
15 variants Other
Infant Length
15 variants Other
Intellectual Developmental Disorder with Abnormal Behavior
15 variants Other
Intestinal Behcet's Disease
15 variants Other
Iowa Type
15 variants Other
Isolated Focal Non-epidermolytic Palmoplantar Keratoderma
15 variants Other
Isthmus-cingulate Cortex Volume
15 variants Other
Itgb1bp2/ptpn6 Protein Level Ratio
15 variants Other
Joint Destruction in Rheumatoid Arthritis (rapid Vs Slow)
15 variants Autoimmune
Joubert Syndrome 30
15 variants Other
Jup-related Disorder
15 variants Other
Juvenile Dermatomyositis
15 variants Other
Juvenile Onset Parkinson Disease 19a
15 variants Neurological
Killer Cell Immunoglobulin-like Receptor 2dl4 Levels
15 variants Other
Lat2/yes1 Protein Level Ratio
15 variants Other
Lead Levels in Blood
15 variants Other
Left Subiculum Volume (body)
15 variants Other
Left Ventricular End Systole Inferoseptal Wall Thickness
15 variants Other
Left Ventricular Obstructive Tract Defect (inherited Effect)
15 variants Other
Levy-hollister Syndrome
15 variants Other
Linolenoylcarnitine (c18:3) Levels
15 variants Other
Lipoprotein (a) - Cholesterol Levels
15 variants Metabolic
Lysophosphatidylethanolamine-o_18:1_[m-h]1-/lysophosphatidylethanolamine-p_18:0_[m-h]1- Levels
15 variants Other
Malignant Lymphoma (non-hodgkin Lymphoma, Multiple Myeloma, or Hodgkin Lymphoma)
15 variants Cancer
Mandibuloacral Dysplasia with Type B Lipodystrophy
15 variants Other
Mannose Levels
15 variants Other
Medial Temporal Thickness (unadjusted For Global Measures)
15 variants Other
Meier-gorlin Syndrome
15 variants Other
Meier-gorlin Syndrome 3
15 variants Other
Meier-gorlin Syndrome 4
15 variants Other
Melanesian Blond Hair
15 variants Other
Metabolic Syndrome (bivariate Traits)
15 variants Metabolic
Metabolonic Lactone Sulfate (x-12063) Levels
15 variants Other
Mgat2-congenital Disorder of Glycosylation
15 variants Other
Microcephalic Primordial Dwarfism Due to Znf335 Deficiency
15 variants Other
Microcephaly 20
15 variants Other
Mild Intellectual Disability
15 variants Other
Mmachc-related Disorder
15 variants Other
Mmut-related Disorder
15 variants Other
Monohexosylceramide (d18:1/24:1) Levels
15 variants Other
Mortality in Sepsis
15 variants Other
Movement Related Adverse Drug Reaction to Aripiprazole in Schizophrenia
15 variants Neurological
Mpdu1-congenital Disorder of Glycosylation
15 variants Other
Multiple Mitochondrial Dysfunctions Syndrome 1
15 variants Other
Multiple Renal Cysts
15 variants Renal
Muscle Weakness
15 variants Other
Myeloblastin Levels
15 variants Other
Neonatal White Matter Microstructure
15 variants Other
Nephrolithiasis Susceptibility Caused By Slc26a1
15 variants Renal
Neurodevelopmental Disorder with Severe Motor Impairment and Absent Language
15 variants Other
Nhlrc3 Protein Levels
15 variants Other
Noncirrhotic
15 variants Other
Nonsyndromic Cleft Lip
15 variants Other
Nonsyndromic Deafness
15 variants Other
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