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Variant-specific associations

rs10153620
log Bayes Factor = <0.0001
Chromosome 2   position 206,060,637  (GRCh37) Explore rs10153620 on Ensembl!
Variant rs10153620 is listed in the   GWAS Catalog  

Hospitalization Episode Statistics (HES)

Self-Reported Statistics (SRS)

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Results table
Term Risk
posterior probability
No effect
posterior probability
Protective
posterior probability
 
N70.1 Chronic salpingitis and oophoritis
0.080 0.920 0.000
N70 Salpingitis and oophoritis
0.041 0.959 0.000
N70.0 Acute salpingitis and oophoritis
0.032 0.968 0.000
N70.9 Salpingitis and oophoritis, unspecified
0.030 0.970 0.000
Q61 Cystic kidney disease
0.000 0.989 0.010
Q61.2 Polycystic kidney, adult type
0.000 0.989 0.011
Q61.3 Polycystic kidney, unspecified
0.000 0.989 0.010
Q61.0 Congenital single renal cyst
0.000 0.991 0.009
K26.4 Chronic or unspecified with haemorrhage
0.000 0.991 0.009
J43.9 Emphysema, unspecified
0.000 0.991 0.009
Q61.9 Cystic kidney disease, unspecified
0.000 0.991 0.009
Q61.5 Medullary cystic kidney
0.000 0.991 0.008
K26 Duodenal ulcer
0.000 0.992 0.008
Q61.8 Other cystic kidney diseases
0.000 0.992 0.008
Q61.4 Renal dysplasia
0.000 0.992 0.008
Q61.1 Polycystic kidney, infantile type
0.000 0.992 0.008
K26.7 Chronic without haemorrhage or perforation
0.000 0.992 0.008
Q21.1 Atrial septal defect
0.008 0.992 0.000
K26.9 Unspecified as acute or chronic, without haemorrhage or perforation
0.000 0.993 0.007
D86.0 Sarcoidosis of lung
0.007 0.993 0.000
D86.9 Sarcoidosis, unspecified
0.007 0.993 0.000
D86 Sarcoidosis
0.007 0.993 0.000
K26.3 Acute without haemorrhage or perforation
0.000 0.993 0.007
N81.5 Vaginal enterocele
0.000 0.993 0.007
M19.91 Arthrosis, unspecified (Shoulder region)
0.007 0.993 0.000
K26.1 Acute with perforation
0.000 0.993 0.006
K26.5 Chronic or unspecified with perforation
0.000 0.994 0.006
D86.3 Sarcoidosis of skin
0.006 0.994 0.000
K26.2 Acute with both haemorrhage and perforation
0.000 0.994 0.006
D86.8 Sarcoidosis of other and combined sites
0.006 0.994 0.000
K26.6 Chronic or unspecified with both haemorrhage and perforation
0.000 0.994 0.006
D86.1 Sarcoidosis of lymph nodes
0.005 0.995 0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.005 0.995 0.000
R94.3 Abnormal results of cardiovascular function studies
0.005 0.995 0.000
Q21 Congenital malformations of cardiac septa
0.005 0.995 0.000
K26.0 Acute with haemorrhage
0.000 0.995 0.005
R52.1 Chronic intractable pain
0.005 0.995 0.000
M62.80 Other specified disorders of muscle (Multiple sites)
0.000 0.995 0.004
M62.8 Other specified disorders of muscle
0.000 0.996 0.004
I05.9 Mitral valve disease, unspecified
0.004 0.996 0.000
Q21.3 Tetralogy of Fallot
0.004 0.996 0.000
M62.89 Other specified disorders of muscle (Site unspecified)
0.000 0.996 0.004
M62.85 Other specified disorders of muscle (Pelvic region and thigh)
0.000 0.996 0.004
Q21.9 Congenital malformation of cardiac septum, unspecified
0.004 0.996 0.000
M62.86 Other specified disorders of muscle (Lower leg)
0.000 0.996 0.004
Q21.8 Other congenital malformations of cardiac septa
0.004 0.996 0.000
Q21.4 Aortopulmonary septal defect
0.004 0.996 0.000
Q21.2 Atrioventricular septal defect
0.004 0.996 0.000
J43 Emphysema
0.000 0.996 0.004
M62.88 Other specified disorders of muscle (Other)
0.000 0.996 0.004
I08.1 Disorders of both mitral and tricuspid valves
0.004 0.996 0.000
K25.7 Chronic without haemorrhage or perforation
0.000 0.996 0.004
Q21.0 Ventricular septal defect
0.004 0.996 0.000
I05 Rheumatic mitral valve diseases
0.004 0.996 0.000
M47.26 Other spondylosis with radiculopathy (Lumbar region)
0.000 0.996 0.004
I47.1 Supraventricular tachycardia
0.003 0.997 0.000
I05.0 Mitral stenosis
0.003 0.997 0.000
M62.87 Other specified disorders of muscle (Ankle and foot)
0.000 0.997 0.003
M62.84 Other specified disorders of muscle (Hand)
0.000 0.997 0.003
M62.83 Other specified disorders of muscle (Forearm)
0.000 0.997 0.003
J43.2 Centrilobular emphysema
0.000 0.997 0.003
M65.43 Radial styloid tenosynovitis [de Quervain] (Forearm)
0.000 0.997 0.003
I05.2 Mitral stenosis with insufficiency
0.003 0.997 0.000
Q20-Q28 Congenital malformations of the circulatory system
0.003 0.997 0.000
Z85.2 Personal history of malignant neoplasm of other respiratory and intrathoracic organs
0.003 0.997 0.000
J43.1 Panlobular emphysema
0.000 0.997 0.003
J43.0 MacLeod's syndrome
0.000 0.997 0.003
M06.00 Seronegative rheumatoid arthritis (Multiple sites)
0.003 0.997 0.000
D18.0 Haemangioma, any site
0.000 0.997 0.003
E04.2 Non-toxic multinodular goitre
0.000 0.997 0.003
M62.82 Other specified disorders of muscle (Upper arm)
0.000 0.997 0.003
Q25 Congenital malformations of great arteries
0.003 0.997 0.000
I05.8 Other mitral valve diseases
0.003 0.997 0.000
Q60-Q64 Congenital malformations of the urinary system
0.001 0.997 0.002
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.003 0.997 0.000
D80-D89 Certain disorders involving the immune mechanism
0.003 0.997 0.000
D89.2 Hypergammaglobulinaemia, unspecified
0.003 0.997 0.000
J43.8 Other emphysema
0.000 0.997 0.003
Q28 Other congenital malformations of circulatory system
0.003 0.997 0.000
Q23 Congenital malformations of aortic and mitral valves
0.003 0.997 0.000
Q25.1 Coarctation of aorta
0.003 0.997 0.000
I05.1 Rheumatic mitral insufficiency
0.003 0.997 0.000
M47.90 Spondylosis, unspecified (Multiple sites in spine)
0.000 0.997 0.003
D89.0 Polyclonal hypergammaglobulinaemia
0.003 0.997 0.000
M62.81 Other specified disorders of muscle (Shoulder region)
0.000 0.997 0.002
Q26 Congenital malformations of great veins
0.002 0.997 0.000
Q22 Congenital malformations of pulmonary and tricuspid valves
0.002 0.997 0.000
Q20 Congenital malformations of cardiac chambers and connexions
0.002 0.997 0.000
Q25.0 Patent ductus arteriosus
0.002 0.997 0.000
G96.1 Disorders of meninges, not elsewhere classified
0.000 0.997 0.002
D26.9 Uterus, unspecified
0.002 0.997 0.000
N89.5 Stricture and atresia of vagina
0.002 0.998 0.000
M65.44 Radial styloid tenosynovitis [de Quervain] (Hand)
0.000 0.998 0.002
Q23.3 Congenital mitral insufficiency
0.002 0.998 0.000
Q23.0 Congenital stenosis of aortic valve
0.002 0.998 0.000
Q25.9 Congenital malformation of great arteries, unspecified
0.002 0.998 0.000
Q25.8 Other congenital malformations of great arteries
0.002 0.998 0.000
Q25.7 Other congenital malformations of pulmonary artery
0.002 0.998 0.000
Q25.6 Stenosis of pulmonary artery
0.002 0.998 0.000
Q25.5 Atresia of pulmonary artery
0.002 0.998 0.000
Q25.3 Stenosis of aorta
0.002 0.998 0.000
Q25.2 Atresia of aorta
0.002 0.998 0.000
M47.99 Spondylosis, unspecified (Site unspecified)
0.000 0.998 0.002
Q25.4 Other congenital malformations of aorta
0.002 0.998 0.000
M65.4 Radial styloid tenosynovitis [de Quervain]
0.000 0.998 0.002
I07.1 Tricuspid insufficiency
0.002 0.998 0.000
D26.1 Corpus uteri
0.002 0.998 0.000
D26.0 Cervix uteri
0.002 0.998 0.000
Q28.2 Arteriovenous malformation of cerebral vessels
0.002 0.998 0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified
0.002 0.998 0.000
D89.3 Immune reconstitution syndrome
0.002 0.998 0.000
D82 Immunodeficiency associated with other major defects
0.002 0.998 0.000
D81 Combined immunodeficiencies
0.002 0.998 0.000
Q24 Other congenital malformations of heart
0.002 0.998 0.000
J35.8 Other chronic diseases of tonsils and adenoids
0.002 0.998 0.000
Q28.3 Other malformations of cerebral vessels
0.002 0.998 0.000
Q28.0 Arteriovenous malformation of precerebral vessels
0.002 0.998 0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
0.001 0.998 0.001
I34.0 Mitral (valve) insufficiency
0.000 0.998 0.002
M47.2 Other spondylosis with radiculopathy
0.000 0.998 0.002
I07 Rheumatic tricuspid valve diseases
0.002 0.998 0.000
Q23.9 Congenital malformation of aortic and mitral valves, unspecified
0.002 0.998 0.000
Q23.8 Other congenital malformations of aortic and mitral valves
0.002 0.998 0.000
Q23.4 Hypoplastic left heart syndrome
0.002 0.998 0.000
Q23.2 Congenital mitral stenosis
0.002 0.998 0.000
Q28.9 Congenital malformation of circulatory system, unspecified
0.002 0.998 0.000
Q28.8 Other specified congenital malformations of circulatory system
0.002 0.998 0.000
Q28.1 Other malformations of precerebral vessels
0.002 0.998 0.000
W22.9 Unspecified place
0.002 0.998 0.000
M62 Other disorders of muscle
0.000 0.998 0.002
Q64 Other congenital malformations of urinary system
0.001 0.998 0.001
G51.0 Bell's palsy
0.000 0.998 0.002
G96.0 Cerebrospinal fluid leak
0.000 0.998 0.002
M88.90 Paget's disease of bone, unspecified (Multiple sites)
0.002 0.998 0.000
I05-I09 Chronic rheumatic heart diseases
0.002 0.998 0.000
Q67.5 Congenital deformity of spine
0.002 0.998 0.000
D89.1 Cryoglobulinaemia
0.002 0.998 0.000
D26 Other benign neoplasms of uterus
0.002 0.998 0.000
M10.97 Gout, unspecified (Ankle and foot)
0.002 0.998 0.000
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified
0.002 0.998 0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions
0.002 0.998 0.000
Q20.6 Isomerism of atrial appendages
0.002 0.998 0.000
Q20.5 Discordant atrioventricular connexion
0.002 0.998 0.000
Q20.4 Double inlet ventricle
0.002 0.998 0.000
Q20.3 Discordant ventriculoarterial connexion
0.002 0.998 0.000
Q20.2 Double outlet left ventricle
0.002 0.998 0.000
Q20.1 Double outlet right ventricle
0.002 0.998 0.000
Q20.0 Common arterial trunk
0.002 0.998 0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified
0.002 0.998 0.000
Q22.8 Other congenital malformations of tricuspid valve
0.002 0.998 0.000
Q22.6 Hypoplastic right heart syndrome
0.002 0.998 0.000
Q22.5 Ebstein's anomaly
0.002 0.998 0.000
Q22.4 Congenital tricuspid stenosis
0.002 0.998 0.000
Q22.3 Other congenital malformations of pulmonary valve
0.002 0.998 0.000
Q22.2 Congenital pulmonary valve insufficiency
0.002 0.998 0.000
Q22.1 Congenital pulmonary valve stenosis
0.002 0.998 0.000
Q22.0 Pulmonary valve atresia
0.002 0.998 0.000
Q26.9 Congenital malformation of great vein, unspecified
0.002 0.998 0.000
Q26.8 Other congenital malformations of great veins
0.002 0.998 0.000
Q26.6 Portal vein-hepatic artery fistula
0.002 0.998 0.000
Q26.5 Anomalous portal venous connexion
0.002 0.998 0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified
0.002 0.998 0.000
Q26.3 Partial anomalous pulmonary venous connexion
0.002 0.998 0.000
Q26.2 Total anomalous pulmonary venous connexion
0.002 0.998 0.000
Q26.1 Persistent left superior vena cava
0.002 0.998 0.000
Q26.0 Congenital stenosis of vena cava
0.002 0.998 0.000
M47.27 Other spondylosis with radiculopathy (Lumbosacral region)
0.000 0.998 0.002
Q24.5 Malformation of coronary vessels
0.002 0.998 0.000
K11.5 Sialolithiasis
0.002 0.998 0.000
L65.9 Nonscarring hair loss, unspecified
0.000 0.998 0.002
Q63 Other congenital malformations of kidney
0.001 0.998 0.001
O47.0 False labour before 37 completed weeks of gestation
0.000 0.998 0.002
D83 Common variable immunodeficiency
0.002 0.998 0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest
0.002 0.998 0.000
E87.8 Other disorders of electrolyte and fluid balance, not elsewhere classified
0.002 0.998 0.000
D89.9 Disorder involving the immune mechanism, unspecified
0.002 0.998 0.000
G96 Other disorders of central nervous system
0.000 0.998 0.002
Q60 Renal agenesis and other reduction defects of kidney
0.001 0.998 0.001
Q27 Other congenital malformations of peripheral vascular system
0.002 0.998 0.000
H65.4 Other chronic nonsuppurative otitis media
0.002 0.998 0.000
Q67.6 Pectus excavatum
0.002 0.998 0.000
M65.49 Radial styloid tenosynovitis [de Quervain]-Site unspec
0.000 0.998 0.002
M65.48 Radial styloid tenosynovitis [de Quervain]-Other
0.000 0.998 0.002
M65.47 Radial styloid tenosynovitis [de Quervain]-Ankle/foot
0.000 0.998 0.002
M65.46 Radial styloid tenosynovitis [de Quervain]-Lower leg
0.000 0.998 0.002
M65.45 Radial styloid tenosynovitis [de Quervain]-Pelvic/thigh
0.000 0.998 0.002
M65.42 Radial styloid tenosynovitis [de Quervain]-Upper arm
0.000 0.998 0.002
M65.41 Radial styloid tenosynovitis [de Quervain]-Shldr region
0.000 0.998 0.002
M65.40 Radial styloid tenosynovitis [de Quervain] (Multiple sites)
0.000 0.998 0.002
O23.4 Unspecified infection of urinary tract in pregnancy
0.000 0.998 0.002
D84 Other immunodeficiencies
0.002 0.998 0.000
I06 Rheumatic aortic valve diseases
0.002 0.998 0.000
I26.9 Pulmonary embolism without mention of acute cor pulmonale
0.002 0.998 0.000
D80 Immunodeficiency with predominantly antibody defects
0.002 0.998 0.000
M10.99 Gout, unspecified (Site unspecified)
0.002 0.998 0.000
H44.2 Degenerative myopia
0.002 0.998 0.000
Q63.0 Accessory kidney
0.002 0.998 0.000
F52.2 Failure of genital response
0.000 0.998 0.002
H92.1 Otorrhoea
0.000 0.998 0.002
Q12.0 Congenital cataract
0.002 0.998 0.000
Q24.6 Congenital heart block
0.002 0.998 0.000
Q24.4 Congenital subaortic stenosis
0.002 0.998 0.000
Q24.3 Pulmonary infundibular stenosis
0.002 0.998 0.000
Q24.2 Cor triatriatum
0.002 0.998 0.000
Q24.1 Levocardia
0.002 0.998 0.000
Q24.0 Dextrocardia
0.002 0.998 0.000
Q63.9 Congenital malformation of kidney, unspecified
0.001 0.998 0.000
D81.9 Combined immunodeficiency, unspecified
0.002 0.998 0.000
D81.8 Other combined immunodeficiencies
0.002 0.998 0.000
D81.7 Major histocompatibility complex class II deficiency
0.002 0.998 0.000
D81.6 Major histocompatibility complex class I deficiency
0.002 0.998 0.000
D81.5 Purine nucleoside phosphorylase [PNP] deficiency
0.002 0.998 0.000
D81.4 Nezelof's syndrome
0.002 0.998 0.000
D81.3 Adenosine deaminase [ADA] deficiency
0.002 0.998 0.000
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
0.002 0.998 0.000
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
0.002 0.998 0.000
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
0.002 0.998 0.000
D82.9 Immunodeficiency associated with major defect, unspecified
0.002 0.998 0.000
D82.8 Immunodeficiency associated with other specified major defects
0.002 0.998 0.000
D82.4 Hyperimmunoglobulin E [IgE] syndrome
0.002 0.998 0.000
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
0.002 0.998 0.000
D82.2 Immunodeficiency with short-limbed stature
0.002 0.998 0.000
D82.1 Di George's syndrome
0.002 0.998 0.000
D82.0 Wiskott-Aldrich syndrome
0.002 0.998 0.000
J38.1 Polyp of vocal cord and larynx
0.002 0.998 0.000
Q23.1 Congenital insufficiency of aortic valve
0.002 0.998 0.000
M25.75 Osteophyte (Pelvic region and thigh)
0.000 0.998 0.002
M47.29 Other spondylosis with radiculopathy (Site unspecified)
0.000 0.998 0.002
M47.28 Other spondylosis with radiculopathy (Sacral and sacrococcygeal region)
0.000 0.998 0.002
M47.25 Other spondylosis with radiculopathy (Thoracolumbar region)
0.000 0.998 0.002
M47.24 Other spondylosis with radiculopathy (Thoracic region)
0.000 0.998 0.002
M47.23 Other spondylosis with radiculopathy (Cervicothoracic region)
0.000 0.998 0.002
M47.21 Other spondylosis with radiculopathy (Occipito-atlanto-axial region)
0.000 0.998 0.002
M47.20 Other spondylosis with radiculopathy (Multiple sites in spine)
0.000 0.998 0.002
I07.9 Tricuspid valve disease, unspecified
0.002 0.998 0.000
I07.8 Other tricuspid valve diseases
0.002 0.998 0.000
I07.2 Tricuspid stenosis with insufficiency
0.002 0.998 0.000
I07.0 Tricuspid stenosis
0.002 0.998 0.000
Q62.8 Other congenital malformations of ureter
0.001 0.998 0.001
Q62.7 Congenital vesico-uretero-renal reflux
0.001 0.998 0.001
Q62.6 Malposition of ureter
0.001 0.998 0.001
Q62.4 Agenesis of ureter
0.001 0.998 0.001
Q62.3 Other obstructive defects of renal pelvis and ureter
0.001 0.998 0.001
Q62.2 Congenital megaloureter
0.001 0.998 0.001
Q62.1 Atresia and stenosis of ureter
0.001 0.998 0.001
Q62.0 Congenital hydronephrosis
0.001 0.998 0.001
K90.9 Intestinal malabsorption, unspecified
0.000 0.998 0.002
M62.5 Muscle wasting and atrophy, not elsewhere classified
0.000 0.998 0.002
M62.4 Contracture of muscle
0.000 0.998 0.002
M62.3 Immobility syndrome (paraplegic)
0.000 0.998 0.002
M62.2 Ischaemic infarction of muscle
0.000 0.998 0.002
M62.1 Other rupture of muscle (nontraumatic)
0.000 0.998 0.002
M62.0 Diastasis of muscle
0.000 0.998 0.002
Q64.9 Congenital malformation of urinary system, unspecified
0.001 0.998 0.001
Q64.8 Other specified congenital malformations of urinary system
0.001 0.998 0.001
Q64.6 Congenital diverticulum of bladder
0.001 0.998 0.001
Q64.5 Congenital absence of bladder and urethra
0.001 0.998 0.001
Q64.4 Malformation of urachus
0.001 0.998 0.001
Q64.2 Congenital posterior urethral valves
0.001 0.998 0.001
Q64.1 Exstrophy of urinary bladder
0.001 0.998 0.001
Q64.0 Epispadias
0.001 0.998 0.001
J30.1 Allergic rhinitis due to pollen
0.002 0.998 0.000
Q12 Congenital lens malformations
0.002 0.998 0.000
I06.0 Rheumatic aortic stenosis
0.002 0.998 0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.002 0.998 0.000
D26.7 Other parts of uterus
0.002 0.998 0.000
E04.9 Non-toxic goitre, unspecified
0.000 0.998 0.002
M62.6 Muscle strain
0.000 0.998 0.002
Q64.7 Other congenital malformations of bladder and urethra
0.001 0.998 0.001
Q64.3 Other atresia and stenosis of urethra and bladder neck
0.001 0.998 0.001
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.002 0.998 0.000
O47.9 False labour, unspecified
0.000 0.998 0.002
Q62.5 Duplication of ureter
0.001 0.998 0.001
F40.2 Specific (isolated) phobias
0.000 0.998 0.002
M47.9 Spondylosis, unspecified
0.000 0.998 0.002
Q63.8 Other specified congenital malformations of kidney
0.001 0.998 0.001
Q63.3 Hyperplastic and giant kidney
0.001 0.998 0.001
O86.4 Pyrexia of unknown origin following delivery
0.002 0.998 0.000
Q67.8 Other congenital deformities of chest
0.002 0.998 0.000
Q67.7 Pectus carinatum
0.002 0.998 0.000
Q67.4 Other congenital deformities of skull, face and jaw
0.002 0.998 0.000
Q67.3 Plagiocephaly
0.002 0.998 0.000
Q67.2 Dolichocephaly
0.002 0.998 0.000
Q67.1 Compression facies
0.002 0.998 0.000
Q67.0 Facial asymmetry
0.002 0.998 0.000
Q18 Other congenital malformations of face and neck
0.002 0.998 0.000
D83.8 Other common variable immunodeficiencies
0.001 0.998 0.000
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells
0.001 0.998 0.000
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
0.001 0.998 0.000
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
0.001 0.998 0.000
M88.9 Paget's disease of bone, unspecified
0.002 0.998 0.000
O47.1 False labour at or after 37 completed weeks of gestation
0.000 0.998 0.002
Q18.0 Sinus, fistula and cyst of branchial cleft
0.002 0.998 0.000
G96.9 Disorder of central nervous system, unspecified
0.000 0.998 0.002
Q60.6 Potter's syndrome
0.001 0.998 0.001
Q60.5 Renal hypoplasia, unspecified
0.001 0.998 0.001
Q60.4 Renal hypoplasia, bilateral
0.001 0.998 0.001
Q60.3 Renal hypoplasia, unilateral
0.001 0.998 0.001
Q60.1 Renal agenesis, bilateral
0.001 0.998 0.001
G93.0 Cerebral cysts
0.000 0.998 0.002
Q24.9 Congenital malformation of the heart, unspecified
0.001 0.998 0.000
I08 Multiple valve diseases
0.002 0.998 0.000
D46.9 Myelodysplastic syndrome, unspecified
0.000 0.998 0.002
Q27.4 Congenital phlebectasia
0.001 0.998 0.000
Q27.2 Other congenital malformations of renal artery
0.001 0.998 0.000
Q27.1 Congenital renal artery stenosis
0.001 0.998 0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery
0.001 0.998 0.000
Q63.2 Ectopic kidney
0.001 0.998 0.001
D84.8 Other specified immunodeficiencies
0.001 0.998 0.000
D84.1 Defects in the complement system
0.001 0.998 0.000
D84.0 Lymphocyte function antigen-1 [LFA-1] defect
0.001 0.998 0.000
I06.9 Rheumatic aortic valve disease, unspecified
0.001 0.998 0.000
I06.8 Other rheumatic aortic valve diseases
0.001 0.998 0.000
I06.2 Rheumatic aortic stenosis with insufficiency
0.001 0.998 0.000
I06.1 Rheumatic aortic insufficiency
0.001 0.998 0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified
0.002 0.998 0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.001 0.998 0.000
D80.8 Other immunodeficiencies with predominantly antibody defects
0.001 0.998 0.000
D80.7 Transient hypogammaglobulinaemia of infancy
0.001 0.998 0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
0.001 0.998 0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]
0.001 0.998 0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]
0.001 0.998 0.000
D80.0 Hereditary hypogammaglobulinaemia
0.001 0.998 0.000
O47 False labour
0.000 0.998 0.002
M62.9 Disorder of muscle, unspecified
0.000 0.998 0.001
Q60.2 Renal agenesis, unspecified
0.001 0.998 0.001
Z95.9 Presence of cardiac and vascular implant and graft, unspecified
0.000 0.998 0.002
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit
0.002 0.998 0.000
B02.9 Zoster without complication
0.000 0.998 0.002
J15.4 Pneumonia due to other streptococci
0.002 0.998 0.000
Q63.1 Lobulated, fused and horseshoe kidney
0.001 0.998 0.001
Q66.3 Other congenital varus deformities of feet
0.002 0.998 0.000
Q79.6 Ehlers-Danlos syndrome
0.002 0.998 0.000
I09 Other rheumatic heart diseases
0.001 0.998 0.000
Q76 Congenital malformations of spine and bony thorax
0.002 0.998 0.000
M62.09 Diastasis of muscle (Site unspecified)
0.000 0.998 0.001
M62.08 Diastasis of muscle (Other)
0.000 0.998 0.001
M62.07 Diastasis of muscle (Ankle and foot)
0.000 0.998 0.001
M62.06 Diastasis of muscle (Lower leg)
0.000 0.998 0.001
M62.05 Diastasis of muscle (Pelvic region and thigh)
0.000 0.998 0.001
M62.04 Diastasis of muscle (Hand)
0.000 0.998 0.001
M62.03 Diastasis of muscle (Forearm)
0.000 0.998 0.001
M62.02 Diastasis of muscle (Upper arm)
0.000 0.998 0.001
M62.01 Diastasis of muscle (Shoulder region)
0.000 0.998 0.001
M62.00 Diastasis of muscle (Multiple sites)
0.000 0.998 0.001
M62.19 Other rupture of muscle (nontraumatic) (Site unspecified)
0.000 0.998 0.001
M62.18 Other rupture of muscle (nontraumatic) (Other)
0.000 0.998 0.001
M62.17 Other rupture of muscle (nontraumatic) (Ankle and foot)
0.000 0.998 0.001
M62.16 Other rupture of muscle (nontraumatic) (Lower leg)
0.000 0.998 0.001
M62.15 Other rupture of muscle (nontraumatic) (Pelvic region and thigh)
0.000 0.998 0.001
M62.14 Other rupture of muscle (nontraumatic) (Hand)
0.000 0.998 0.001
M62.13 Other rupture of muscle (nontraumatic) (Forearm)
0.000 0.998 0.001
M62.12 Other rupture of muscle (nontraumatic) (Upper arm)
0.000 0.998 0.001
M62.11 Other rupture of muscle (nontraumatic) (Shoulder region)
0.000 0.998 0.001
M62.10 Other rupture of muscle (nontraumatic) (Multiple sites)
0.000 0.998 0.001
M62.29 Ischaemic infarction of muscle (Site unspecified)
0.000 0.998 0.001
M62.28 Ischaemic infarction of muscle (Other)
0.000 0.998 0.001
M62.27 Ischaemic infarction of muscle (Ankle and foot)
0.000 0.998 0.001
M62.26 Ischaemic infarction of muscle (Lower leg)
0.000 0.998 0.001
M62.25 Ischaemic infarction of muscle (Pelvic region and thigh)
0.000 0.998 0.001
M62.24 Ischaemic infarction of muscle (Hand)
0.000 0.998 0.001
M62.23 Ischaemic infarction of muscle (Forearm)
0.000 0.998 0.001
M62.22 Ischaemic infarction of muscle (Upper arm)
0.000 0.998 0.001
M62.21 Ischaemic infarction of muscle (Shoulder region)
0.000 0.998 0.001
M62.20 Ischaemic infarction of muscle (Multiple sites)
0.000 0.998 0.001
M62.39 Immobility syndrome (paraplegic) (Site unspecified)
0.000 0.998 0.001
M62.38 Immobility syndrome (paraplegic) (Other)
0.000 0.998 0.001
M62.37 Immobility syndrome (paraplegic) (Ankle and foot)
0.000 0.998 0.001
M62.36 Immobility syndrome (paraplegic) (Lower leg)
0.000 0.998 0.001
M62.35 Immobility syndrome (paraplegic) (Pelvic region and thigh)
0.000 0.998 0.001
M62.34 Immobility syndrome (paraplegic) (Hand)
0.000 0.998 0.001
M62.33 Immobility syndrome (paraplegic) (Forearm)
0.000 0.998 0.001
M62.32 Immobility syndrome (paraplegic) (Upper arm)
0.000 0.998 0.001
M62.31 Immobility syndrome (paraplegic) (Shoulder region)
0.000 0.998 0.001
M62.30 Immobility syndrome (paraplegic) (Multiple sites)
0.000 0.998 0.001
M62.49 Contracture of muscle (Site unspecified)
0.000 0.998 0.001
M62.48 Contracture of muscle (Other)
0.000 0.998 0.001
M62.47 Contracture of muscle (Ankle and foot)
0.000 0.998 0.001
M62.46 Contracture of muscle (Lower leg)
0.000 0.998 0.001
M62.45 Contracture of muscle (Pelvic region and thigh)
0.000 0.998 0.001
M62.44 Contracture of muscle (Hand)
0.000 0.998 0.001
M62.43 Contracture of muscle (Forearm)
0.000 0.998 0.001
M62.42 Contracture of muscle (Upper arm)
0.000 0.998 0.001
M62.41 Contracture of muscle (Shoulder region)
0.000 0.998 0.001
M62.40 Contracture of muscle (Multiple sites)
0.000 0.998 0.001
M62.59 Muscle wasting and atrophy, not elsewhere classified (Site unspecified)
0.000 0.998 0.001
M62.58 Muscle wasting and atrophy, not elsewhere classified (Other)
0.000 0.998 0.001
M62.57 Muscle wasting and atrophy, not elsewhere classified (Ankle and foot)
0.000 0.998 0.001
M62.56 Muscle wasting and atrophy, not elsewhere classified (Lower leg)
0.000 0.998 0.001
M62.55 Muscle wasting and atrophy, not elsewhere classified (Pelvic region and thigh)
0.000 0.998 0.001
M62.54 Muscle wasting and atrophy, not elsewhere classified (Hand)
0.000 0.998 0.001
M62.53 Muscle wasting and atrophy, not elsewhere classified (Forearm)
0.000 0.998 0.001
M62.52 Muscle wasting and atrophy, not elsewhere classified (Upper arm)
0.000 0.998 0.001
M62.51 Muscle wasting and atrophy, not elsewhere classified (Shoulder region)
0.000 0.998 0.001
M62.50 Muscle wasting and atrophy, not elsewhere classified (Multiple sites)
0.000 0.998 0.001
M88.95 Paget's disease of bone, unspecified (Pelvic region and thigh)
0.001 0.998 0.000
C18.4 Transverse colon
0.000 0.998 0.002
Q27.8 Other specified congenital malformations of peripheral vascular system
0.001 0.998 0.000
D80.1 Nonfamilial hypogammaglobulinaemia
0.001 0.998 0.000
Q12.9 Congenital lens malformation, unspecified
0.001 0.998 0.000
Q12.8 Other congenital lens malformations
0.001 0.998 0.000
Q12.4 Spherophakia
0.001 0.998 0.000
Q12.3 Congenital aphakia
0.001 0.998 0.000
Q12.2 Coloboma of lens
0.001 0.998 0.000
Q12.1 Congenital displaced lens
0.001 0.998 0.000
Q76.1 Klippel-Feil syndrome
0.001 0.998 0.000
M62.69 Muscle strain (Site unspecified)
0.000 0.998 0.001
M62.68 Muscle strain (Other)
0.000 0.998 0.001
M62.67 Muscle strain (Ankle and foot)
0.000 0.998 0.001
M62.65 Muscle strain (Pelvic region and thigh)
0.000 0.998 0.001
M62.64 Muscle strain (Hand)
0.000 0.998 0.001
M62.63 Muscle strain (Forearm)
0.000 0.998 0.001
M62.62 Muscle strain (Upper arm)
0.000 0.998 0.001
M62.61 Muscle strain (Shoulder region)
0.000 0.998 0.001
M62.60 Muscle strain (Multiple sites)
0.000 0.998 0.001
G96.8 Other specified disorders of central nervous system
0.000 0.998 0.001
Q17 Other congenital malformations of ear
0.001 0.998 0.000
Q16 Congenital malformations of ear causing impairment of hearing
0.001 0.998 0.000
Q15 Other congenital malformations of eye
0.001 0.998 0.000
Q14 Congenital malformations of posterior segment of eye
0.001 0.998 0.000
Q13 Congenital malformations of anterior segment of eye
0.001 0.998 0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos
0.001 0.998 0.000
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine
0.001 0.998 0.000
Q75 Other congenital malformations of skull and face bones
0.001 0.998 0.000
Q73 Reduction defects of unspecified limb
0.001 0.998 0.000
Q72 Reduction defects of lower limb
0.001 0.998 0.000
Q71 Reduction defects of upper limb
0.001 0.998 0.000
Q70 Syndactyly
0.001 0.998 0.000
Q69 Polydactyly
0.001 0.998 0.000
Q68 Other congenital musculoskeletal deformities
0.001 0.998 0.000
M89.86 Other specified disorders of bone (Lower leg)
0.002 0.998 0.000
D83.9 Common variable immunodeficiency, unspecified
0.001 0.998 0.000
J95.8 Other postprocedural respiratory disorders
0.000 0.998 0.002
K27.9 Unspecified as acute or chronic, without haemorrhage or perforation
0.002 0.998 0.000
Q78 Other osteochondrodysplasias
0.001 0.998 0.000
Q66 Congenital deformities of feet
0.002 0.998 0.000
M47.93 Spondylosis, unspecified (Cervicothoracic region)
0.000 0.998 0.001
M47.91 Spondylosis, unspecified (Occipito-atlanto-axial region)
0.000 0.998 0.001
M88.99 Paget's disease of bone, unspecified (Site unspecified)
0.001 0.998 0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses
0.001 0.998 0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]
0.001 0.998 0.000
E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
0.002 0.998 0.000
Q18.9 Congenital malformation of face and neck, unspecified
0.001 0.998 0.000
Q18.8 Other specified congenital malformations of face and neck
0.001 0.998 0.000
Q18.7 Microcheilia
0.001 0.998 0.000
Q18.6 Macrocheilia
0.001 0.998 0.000
Q18.5 Microstomia
0.001 0.998 0.000
Q18.4 Macrostomia
0.001 0.998 0.000
Q18.3 Webbing of neck
0.001 0.998 0.000
Q18.2 Other branchial cleft malformations
0.001 0.998 0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.002 0.998 0.000
M06.06 Seronegative rheumatoid arthritis (Lower leg)
0.001 0.998 0.000
M47.22 Other spondylosis with radiculopathy (Cervical region)
0.000 0.998 0.001
M62.66 Muscle strain (Lower leg)
0.000 0.998 0.001
M88.98 Paget's disease of bone, unspecified (Other)
0.001 0.998 0.000
M88.97 Paget's disease of bone, unspecified (Ankle and foot)
0.001 0.998 0.000
M88.96 Paget's disease of bone, unspecified (Lower leg)
0.001 0.998 0.000
M88.94 Paget's disease of bone, unspecified (Hand)
0.001 0.998 0.000
M88.93 Paget's disease of bone, unspecified (Forearm)
0.001 0.998 0.000
M88.92 Paget's disease of bone, unspecified (Upper arm)
0.001 0.998 0.000
M88.91 Paget's disease of bone, unspecified (Shoulder region)
0.001 0.998 0.000
M06.0 Seronegative rheumatoid arthritis
0.002 0.998 0.000
M67.8 Other specified disorders of synovium and tendon
0.000 0.998 0.002
Q27.9 Congenital malformation of peripheral vascular system, unspecified
0.001 0.998 0.000
Q76.5 Cervical rib
0.001 0.998 0.000
G99.0 Autonomic neuropathy in endocrine and metabolic diseases
0.000 0.998 0.001
O21.0 Mild hyperemesis gravidarum
0.000 0.998 0.002
Q10.0 Congenital ptosis
0.001 0.998 0.000
Q18.1 Preauricular sinus and cyst
0.001 0.998 0.000
Q60.0 Renal agenesis, unilateral
0.001 0.998 0.001
I34.2 Nonrheumatic mitral (valve) stenosis
0.000 0.998 0.001
O86.2 Urinary tract infection following delivery
0.001 0.998 0.000
K25.0 Acute with haemorrhage
0.000 0.998 0.001
Q78.2 Osteopetrosis
0.001 0.998 0.000
Q79.9 Congenital malformation of musculoskeletal system, unspecified
0.001 0.998 0.000
Q79.5 Other congenital malformations of abdominal wall
0.001 0.998 0.000
Q79.4 Prune belly syndrome
0.001 0.998 0.000
Q79.3 Gastroschisis
0.001 0.998 0.000
Q79.2 Exomphalos
0.001 0.998 0.000
Q79.1 Other congenital malformations of diaphragm
0.001 0.998 0.000
Q79.0 Congenital diaphragmatic hernia
0.001 0.998 0.000
Q74 Other congenital malformations of limb(s)
0.001 0.998 0.000
R54 Senility
0.000 0.998 0.001
D84.9 Immunodeficiency, unspecified
0.001 0.999 0.001
G90.3 Multisystem degeneration
0.000 0.999 0.001
Q24.8 Other specified congenital malformations of heart
0.001 0.999 0.000
Y91.9 Alcohol involvement, not otherwise specified
0.000 0.999 0.001
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.001 0.999 0.000
M06.07 Seronegative rheumatoid arthritis (Ankle and foot)
0.001 0.999 0.000
M47.94 Spondylosis, unspecified (Thoracic region)
0.000 0.999 0.001
M62.98 Disorder of muscle, unspecified (Other)
0.000 0.999 0.001
M62.97 Disorder of muscle, unspecified (Ankle and foot)
0.000 0.999 0.001
M62.95 Disorder of muscle, unspecified (Pelvic region and thigh)
0.000 0.999 0.001
M62.94 Disorder of muscle, unspecified (Hand)
0.000 0.999 0.001
M62.93 Disorder of muscle, unspecified (Forearm)
0.000 0.999 0.001
M62.92 Disorder of muscle, unspecified (Upper arm)
0.000 0.999 0.001
M62.91 Disorder of muscle, unspecified (Shoulder region)
0.000 0.999 0.001
M62.90 Disorder of muscle, unspecified (Multiple sites)
0.000 0.999 0.001
Q10.7 Congenital malformation of orbit
0.001 0.999 0.000
Q10.6 Other congenital malformations of lachrymal apparatus
0.001 0.999 0.000

This table lists the top 500 terms ordered by p(effect).

The full results table can be downloaded from this page.