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)
Aparc-dktatlas Lh Volume Pericalcarine
Aparc-dktatlas Rh Area Lingual
Aparc-pial Rh Area Lingual
Aparc-pial Rh Area Pericalcarine
Apc2-related Disorder
Aplasia Cutis-enamel Dysplasia Syndrome
Aplasia/hypoplasia of the Cerebellum
Apo-ciii1/apo-ciii2 Ratio
Apolipoprotein A-iv Levels
Apolipoprotein C-ii Levels
Apolipoprotein C-iii Deficiency
Apom/mcam Protein Level Ratio
Appendicitis (phecode 540.1)
Arabinose Levels in Elite Athletes
Arabonate/xylonate Levels
Arachidonoylcarnitine (c20:4) Levels in Elite Athletes
Argininate Levels in Elite Athletes
Arhgef12/bank1 Protein Level Ratio
Arterial Stiffness (brachial-femoral Pulse Wave Velocity)
Arteriovenous Malformation
Arthrogryposis Multiplex Congenita 5
Aseg Global Volume 4th-ventricle
Aseg Global Volume Ventriclechoroid
Aseg Lh Intensity Caudate
Aseg Lh Volume Cerebellum-cortex
Aseg Rh Intensity Pallidum
Aseg Rh Volume Pallidum
Aseptic Necrosis of Bone (phecode 733.4)
Asparagine Levels in Elite Athletes
Asperger Disorder
Asporin Levels
Asymptomatic Hyperuricaemia (age <50)
Atelis Syndrome 1
Athlete's Foot (phecode 110.12)
Atox1/tmsb10 Protein Level Ratio
Atp8a2-related Disorder
Atrial Standstill 2
Atrioventricular Conduction
Atrophic Gastritis (phecode 535.2)
Atrophy/degeneration Affecting the Central Nervous System
Atxn10 Protein Levels
Atypical Endometrial Hyperplasia
Atypical Severe Combined Immunodeficiency Due to Complete Rag1/2 Deficiency
Autoinflammation with Episodic Fever and Lymphadenopathy
Autophagic Vacuolar
Autosomal Dominant 67
Autosomal Dominant 74
Autosomal Dominant 75
Autosomal Dominant 80
Autosomal Dominant Ichthyosis Vulgaris
Autosomal Dominant Nonsyndromic Hearing Loss 27
Autosomal Dominant Popliteal Pterygium Syndrome
Autosomal Dominant Sensory Ataxia 1
Autosomal Recessive 119
Autosomal Recessive 74
Autosomal Recessive Abca4-related Disorders
Autosomal Recessive Dyskeratosis Congenita 4
Autosomal Recessive Inheritance
Autosomal Recessive Nonsyndromic Hearing Loss 124
Autosomal Recessive Nonsyndromic Hearing Loss 39
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