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)
Histidine-rich Glycoprotein Levels
Hpse Protein Levels
Hsd10 Mitochondrial Disease
Hypercoagulable State (phecode 286.8)
Hyperlysinemia
Hypermanganesemia with Dystonia
Hypersulfaturia
Hypertrophic Cardiomyopathy 8
Hyperuricemia in Low Vitamin B6 Intake
Hypomyelinating Leukodystrophy 9
Idiopathic Downbeat Nystagmus
Ifih1-related Disorder
Impaired Intellectual Development
Inattentive Symptoms
Infant Length
Intellectual Developmental Disorder with Abnormal Behavior
Intestinal Behcet's Disease
Iowa Type
Isolated Focal Non-epidermolytic Palmoplantar Keratoderma
Isthmus-cingulate Cortex Volume
Itgb1bp2/ptpn6 Protein Level Ratio
Joubert Syndrome 30
Jup-related Disorder
Juvenile Dermatomyositis
Killer Cell Immunoglobulin-like Receptor 2dl4 Levels
Lat2/yes1 Protein Level Ratio
Lead Levels in Blood
Left Subiculum Volume (body)
Left Ventricular End Systole Inferoseptal Wall Thickness
Left Ventricular Obstructive Tract Defect (inherited Effect)
Levy-hollister Syndrome
Linolenoylcarnitine (c18:3) Levels
Lysophosphatidylethanolamine-o_18:1_[m-h]1-/lysophosphatidylethanolamine-p_18:0_[m-h]1- Levels
Mandibuloacral Dysplasia with Type B Lipodystrophy
Mannose Levels
Medial Temporal Thickness (unadjusted For Global Measures)
Meier-gorlin Syndrome
Meier-gorlin Syndrome 3
Meier-gorlin Syndrome 4
Melanesian Blond Hair
Metabolonic Lactone Sulfate (x-12063) Levels
Mgat2-congenital Disorder of Glycosylation
Microcephalic Primordial Dwarfism Due to Znf335 Deficiency
Microcephaly 20
Mild Intellectual Disability
Mmachc-related Disorder
Mmut-related Disorder
Monohexosylceramide (d18:1/24:1) Levels
Mortality in Sepsis
Mpdu1-congenital Disorder of Glycosylation
Multiple Mitochondrial Dysfunctions Syndrome 1
Muscle Weakness
Myeloblastin Levels
Neonatal White Matter Microstructure
Neurodevelopmental Disorder with Severe Motor Impairment and Absent Language
Nhlrc3 Protein Levels
Noncirrhotic
Nonsyndromic Cleft Lip
Nonsyndromic Deafness
Noonan Syndrome 6
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