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)
Marzipan Liking
Masp1-related Disorder
Mast/stem Cell Growth Factor Receptor Kit Levels
Matrilin-3 Levels
Matrilysin Levels
Mean Arterial Pressure X Low Social Support Interaction (2df Test)
Mean Reticulocyte Volume Variance
Meckel Syndrome 14
Mecr Protein Levels
Med18/sh2b3 Protein Level Ratio
Medial Thalamic Nuclei Volume
Mednik Syndrome
Meier-gorlin Syndrome 5
Melanocyte Protein Pmel Levels
Memory For Intentions Screening Test (mist) Delay (mist Delay)
Menarche and Menopause (age At Onset)
Meningococcal C Functional Antibody Titers Post Childhood Immunization
Mental Deterioration
Merkel Cell Polyomavirus Vp1 Antibody Levels
Mesangiocapillary Glomerulonephritis
Metabolite Levels (1-stearoyl-2-arachidonoyl-gpe (18:0/20:4); C38:4 Pe)
Metabolite Levels (4-androsten-3alpha,17alpha-diol Monosulfate (3); Androstenediol (3alpha, 17alpha) Monosulfate (3))
Metabolite Levels (androsterone Sulfate)
Metabolite Levels (cys-gly, Oxidized)
Metabolite Levels (cysteine-glutathione Disulfide)
Metabolite Levels (glutarylcarnitine (c5); Glutarylcarnitine (c5-dc); C5-dc Carnitine; C5_dc_carnitine)
Metabolite Levels (glycocholenate Sulfate)
Metabolite Levels (hexadecanedioate; Hexadecanedioate (c16-dc))
Metabolite Levels (imidazole Lactate; Imidazolelactate)
Metabolite Levels (proline)
Metabolite Levels (propionylcarnitine; Propionylcarnitine (c3); C3 Carnitine; C3_carnitine)
Metabolite Peak Levels (qi9680)
Methylglutarylcarnitine Levels
Methylmalonic Aciduria and Homocystinuria
Methylsuccinoylcarnitine Levels
Mgll Protein Levels
Microcephalic Osteodysplastic Dysplasia
Microcephaly 14
Microcephaly-micromelia Syndrome
Microphthalmia/coloboma 11
Midface Hypoplasia
Mitd1/rhoc Protein Level Ratio
Mitochondrial Complex Iii Deficiency Nuclear Type 5
Mitochondrial Dna Copy Number (white Blood Cells)
Mitochondrial Dna Deletion Syndrome with Progressive Myopathy
Mitochondrial Dna Heteroplasmy (chrm:16183:ac:a Case-only Heteroplasmy)
Mitochondrial Dna Heteroplasmy (chrm:302:a:acc Case-only Heteroplasmy)
Mitochondrial Pyruvate Carrier Deficiency
Mitochondrial Type 1
Mmp8/mmp9 Protein Level Ratio
Mpig6b/plxna4 Protein Level Ratio
Msra/serpinb1 Protein Level Ratio
Muenke Syndrome
Multimerin-2 Levels (mmrn2.11895.21.3)
Multiminicore Myopathy
Multiple Inositol Polyphosphate Phosphatase 1 Levels
Multiple Synostoses Syndrome 3
Myalgia
Mycn-related Disorder
Mydgf Protein Levels
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