TreeWAS – Variant ID: rs13015955

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
N13.3 Other and unspecified hydronephrosis	0.000	0.840	0.160
N13 Obstructive and reflux uropathy	0.000	0.851	0.149
N13.5 Kinking and stricture of ureter without hydronephrosis	0.000	0.856	0.144
N13.1 Hydronephrosis with ureteral stricture, not elsewhere classified	0.000	0.869	0.131
N13.2 Hydronephrosis with renal and ureteral calculous obstruction	0.000	0.869	0.131
N13.6 Pyonephrosis	0.000	0.871	0.129
N13.7 Vesicoureteral-reflux-associated uropathy	0.000	0.884	0.116
N13.0 Hydronephrosis with ureteropelvic junction obstruction	0.000	0.888	0.112
N13.4 Hydroureter	0.000	0.906	0.094
N13.8 Other obstructive and reflux uropathy	0.000	0.945	0.055
N73.6 Female pelvic peritoneal adhesions	0.000	0.958	0.042
N13.9 Obstructive and reflux uropathy, unspecified	0.001	0.960	0.040
Q20-Q28 Congenital malformations of the circulatory system	0.038	0.962	0.000
Q21.0 Ventricular septal defect	0.038	0.962	0.000
Q21 Congenital malformations of cardiac septa	0.038	0.962	0.000
N73 Other female pelvic inflammatory diseases	0.000	0.963	0.037
Q25 Congenital malformations of great arteries	0.036	0.964	0.000
Q24 Other congenital malformations of heart	0.035	0.965	0.000
Q27 Other congenital malformations of peripheral vascular system	0.035	0.965	0.000
N73.9 Female pelvic inflammatory disease, unspecified	0.000	0.967	0.033
Q23 Congenital malformations of aortic and mitral valves	0.032	0.968	0.000
Q21.9 Congenital malformation of cardiac septum, unspecified	0.032	0.968	0.000
Q24.9 Congenital malformation of the heart, unspecified	0.032	0.968	0.000
Q25.1 Coarctation of aorta	0.031	0.969	0.000
Q27.3 Peripheral arteriovenous malformation	0.031	0.969	0.000
Q24.8 Other specified congenital malformations of heart	0.030	0.970	0.000
Q21.3 Tetralogy of Fallot	0.030	0.970	0.000
N73.5 Female pelvic peritonitis, unspecified	0.000	0.970	0.029
R79.9 Abnormal finding of blood chemistry, unspecified	0.029	0.971	0.000
Q25.0 Patent ductus arteriosus	0.029	0.971	0.000
N73.1 Chronic parametritis and pelvic cellulitis	0.000	0.971	0.029
Q25.4 Other congenital malformations of aorta	0.029	0.971	0.000
Q22 Congenital malformations of pulmonary and tricuspid valves	0.028	0.972	0.000
Q26 Congenital malformations of great veins	0.028	0.972	0.000
Q20 Congenital malformations of cardiac chambers and connexions	0.028	0.972	0.000
N70-N77 Inflammatory diseases of female pelvic organs	0.000	0.972	0.028
Q21.8 Other congenital malformations of cardiac septa	0.027	0.972	0.000
Q21.4 Aortopulmonary septal defect	0.027	0.972	0.000
Q21.2 Atrioventricular septal defect	0.027	0.972	0.000
Q25.3 Stenosis of aorta	0.027	0.972	0.000
Q23.0 Congenital stenosis of aortic valve	0.027	0.973	0.000
Q27.8 Other specified congenital malformations of peripheral vascular system	0.027	0.973	0.000
N73.4 Female chronic pelvic peritonitis	0.000	0.973	0.026
N73.3 Female acute pelvic peritonitis	0.000	0.973	0.026
N73.2 Unspecified parametritis and pelvic cellulitis	0.000	0.973	0.026
Q27.9 Congenital malformation of peripheral vascular system, unspecified	0.026	0.974	0.000
N71 Inflammatory disease of uterus, except cervix	0.000	0.974	0.026
Q25.6 Stenosis of pulmonary artery	0.026	0.974	0.000
Q25.9 Congenital malformation of great arteries, unspecified	0.026	0.974	0.000
Q25.8 Other congenital malformations of great arteries	0.026	0.974	0.000
Q25.7 Other congenital malformations of pulmonary artery	0.026	0.974	0.000
Q25.5 Atresia of pulmonary artery	0.026	0.974	0.000
Q25.2 Atresia of aorta	0.026	0.974	0.000
Q24.6 Congenital heart block	0.025	0.975	0.000
Q24.4 Congenital subaortic stenosis	0.025	0.975	0.000
Q24.3 Pulmonary infundibular stenosis	0.025	0.975	0.000
Q24.2 Cor triatriatum	0.025	0.975	0.000
Q24.1 Levocardia	0.025	0.975	0.000
Q24.0 Dextrocardia	0.025	0.975	0.000
Q27.4 Congenital phlebectasia	0.025	0.975	0.000
Q27.2 Other congenital malformations of renal artery	0.025	0.975	0.000
Q27.1 Congenital renal artery stenosis	0.025	0.975	0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery	0.025	0.975	0.000
N73.8 Other specified female pelvic inflammatory diseases	0.000	0.976	0.024
N71.9 Inflammatory disease of uterus, unspecified	0.000	0.976	0.024
N72 Inflammatory disease of cervix uteri	0.000	0.976	0.024
N76 Other inflammation of vagina and vulva	0.000	0.976	0.024
Q23.1 Congenital insufficiency of aortic valve	0.024	0.976	0.000
N76.2 Acute vulvitis	0.000	0.976	0.024
Q23.9 Congenital malformation of aortic and mitral valves, unspecified	0.023	0.977	0.000
Q23.8 Other congenital malformations of aortic and mitral valves	0.023	0.977	0.000
Q23.4 Hypoplastic left heart syndrome	0.023	0.977	0.000
Q23.3 Congenital mitral insufficiency	0.023	0.977	0.000
Q23.2 Congenital mitral stenosis	0.023	0.977	0.000
N71.1 Chronic inflammatory disease of uterus	0.000	0.978	0.022
Q22.1 Congenital pulmonary valve stenosis	0.021	0.978	0.000
Q28 Other congenital malformations of circulatory system	0.021	0.979	0.000
Q21.1 Atrial septal defect	0.021	0.979	0.000
Q22.9 Congenital malformation of tricuspid valve, unspecified	0.020	0.979	0.000
Q22.8 Other congenital malformations of tricuspid valve	0.020	0.979	0.000
Q22.6 Hypoplastic right heart syndrome	0.020	0.979	0.000
Q22.5 Ebstein's anomaly	0.020	0.979	0.000
Q22.4 Congenital tricuspid stenosis	0.020	0.979	0.000
Q22.3 Other congenital malformations of pulmonary valve	0.020	0.979	0.000
Q22.2 Congenital pulmonary valve insufficiency	0.020	0.979	0.000
Q22.0 Pulmonary valve atresia	0.020	0.979	0.000
Q24.5 Malformation of coronary vessels	0.020	0.979	0.000
N76.6 Ulceration of vulva	0.000	0.980	0.020
Q20.9 Congenital malformation of cardiac chambers and connexions, unspecified	0.020	0.980	0.000
Q20.8 Other congenital malformations of cardiac chambers and connexions	0.020	0.980	0.000
Q20.6 Isomerism of atrial appendages	0.020	0.980	0.000
Q20.5 Discordant atrioventricular connexion	0.020	0.980	0.000
Q20.4 Double inlet ventricle	0.020	0.980	0.000
Q20.3 Discordant ventriculoarterial connexion	0.020	0.980	0.000
Q20.2 Double outlet left ventricle	0.020	0.980	0.000
Q20.1 Double outlet right ventricle	0.020	0.980	0.000
Q20.0 Common arterial trunk	0.020	0.980	0.000
Q26.9 Congenital malformation of great vein, unspecified	0.020	0.980	0.000
Q26.8 Other congenital malformations of great veins	0.020	0.980	0.000
Q26.6 Portal vein-hepatic artery fistula	0.020	0.980	0.000
Q26.5 Anomalous portal venous connexion	0.020	0.980	0.000
Q26.4 Anomalous pulmonary venous connexion, unspecified	0.020	0.980	0.000
Q26.3 Partial anomalous pulmonary venous connexion	0.020	0.980	0.000
Q26.2 Total anomalous pulmonary venous connexion	0.020	0.980	0.000
Q26.1 Persistent left superior vena cava	0.020	0.980	0.000
Q26.0 Congenital stenosis of vena cava	0.020	0.980	0.000
N74 Female pelvic inflammatory disorders in diseases classified elsewhere	0.000	0.980	0.020
N70 Salpingitis and oophoritis	0.000	0.980	0.020
N73.0 Acute parametritis and pelvic cellulitis	0.000	0.981	0.019
N71.0 Acute inflammatory disease of uterus	0.000	0.981	0.019
N70.9 Salpingitis and oophoritis, unspecified	0.000	0.982	0.018
N76.3 Subacute and chronic vulvitis	0.000	0.982	0.018
N76.5 Ulceration of vagina	0.000	0.982	0.017
N76.8 Other specified inflammation of vagina and vulva	0.000	0.984	0.016
N76.0 Acute vaginitis	0.000	0.984	0.016
Q28.0 Arteriovenous malformation of precerebral vessels	0.015	0.984	0.000
N76.1 Subacute and chronic vaginitis	0.000	0.984	0.015
N77 Vulvovaginal ulceration and inflammation in diseases classified elsewhere	0.000	0.984	0.015
Q28.9 Congenital malformation of circulatory system, unspecified	0.015	0.985	0.000
Q28.8 Other specified congenital malformations of circulatory system	0.015	0.985	0.000
Q28.1 Other malformations of precerebral vessels	0.015	0.985	0.000
Q28.3 Other malformations of cerebral vessels	0.015	0.985	0.000
N74.8 Female pelvic inflammatory disorders in other diseases classified elsewhere	0.000	0.985	0.014
N74.4 Female chlamydial pelvic inflammatory disease	0.000	0.985	0.014
N74.3 Female gonococcal pelvic inflammatory disease	0.000	0.985	0.014
N74.2 Female syphilitic pelvic inflammatory disease	0.000	0.985	0.014
N74.1 Female tuberculous pelvic inflammatory disease	0.000	0.985	0.014
N74.0 Tuberculous infection of cervix uteri	0.000	0.985	0.014
N70.1 Chronic salpingitis and oophoritis	0.000	0.988	0.012
N77.8 Vulvovaginal ulceration and inflammation in other diseases classified elsewhere	0.000	0.989	0.011
N77.0 Ulceration of vulva in infectious and parasitic diseases classified elsewhere	0.000	0.989	0.011
N75 Diseases of Bartholin's gland	0.000	0.989	0.011
N70.0 Acute salpingitis and oophoritis	0.000	0.989	0.011
H90.5 Sensorineural hearing loss, unspecified	0.000	0.990	0.010
N48.8 Other specified disorders of penis	0.000	0.991	0.009
N48.1 Balanoposthitis	0.000	0.991	0.009
N48.2 Other inflammatory disorders of penis	0.000	0.991	0.009
N48 Other disorders of penis	0.000	0.991	0.009
N75.9 Disease of Bartholin's gland, unspecified	0.000	0.992	0.008
Q28.2 Arteriovenous malformation of cerebral vessels	0.008	0.992	0.001
N10-N16 Renal tubulo-interstitial diseases	0.000	0.992	0.008
N48.4 Impotence of organic origin	0.000	0.992	0.008
N76.4 Abscess of vulva	0.000	0.992	0.008
N75.0 Cyst of Bartholin's gland	0.000	0.992	0.008
S60.9 Superficial injury of wrist and hand, unspecified	0.008	0.992	0.000
N75.8 Other diseases of Bartholin's gland	0.000	0.992	0.008
R79 Other abnormal findings of blood chemistry	0.007	0.993	0.000
N48.0 Leukoplakia of penis	0.000	0.993	0.007
M54.46 Lumbago with sciatica (Lumbar region)	0.007	0.993	0.000
N77.1 Vaginitis, vulvitis and vulvovaginitis in infectious and parasitic diseases classified elsewhere	0.000	0.993	0.007
N48.3 Priapism	0.000	0.994	0.006
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.006	0.994	0.000
Q43.0 Meckel's diverticulum	0.006	0.994	0.000
Q43 Other congenital malformations of intestine	0.006	0.994	0.000
Q38-Q45 Other congenital malformations of the digestive system	0.006	0.994	0.000
N48.5 Ulcer of penis	0.000	0.994	0.006
C79.5 Secondary malignant neoplasm of bone and bone marrow	0.000	0.994	0.006
R79.0 Abnormal level of blood mineral	0.006	0.994	0.000
N14 Drug- and heavy-metal-induced tubulo-interstitial and tubular conditions	0.000	0.994	0.006
N48.9 Disorder of penis, unspecified	0.000	0.994	0.006
N16 Renal tubulo-interstitial disorders in diseases classified elsewhere	0.000	0.994	0.005
N15 Other renal tubulo-interstitial diseases	0.000	0.995	0.005
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.005	0.995	0.000
N11 Chronic tubulo-interstitial nephritis	0.000	0.995	0.005
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system	0.005	0.995	0.000
Q43.3 Congenital malformations of intestinal fixation	0.005	0.995	0.000
Q39 Congenital malformations of oesophagus	0.005	0.995	0.000
D13.2 Duodenum	0.000	0.995	0.005
Q30-Q34 Congenital malformations of the respiratory system	0.005	0.995	0.000
Q35-Q37 Cleft lip and cleft palate	0.005	0.995	0.000
Q40 Other congenital malformations of upper alimentary tract	0.005	0.995	0.000
Q76 Congenital malformations of spine and bony thorax	0.005	0.995	0.000
Q45 Other congenital malformations of digestive system	0.005	0.995	0.000
Q43.7 Persistent cloaca	0.005	0.995	0.000
Q43.6 Congenital fistula of rectum and anus	0.005	0.995	0.000
Q43.5 Ectopic anus	0.005	0.995	0.000
Q43.4 Duplication of intestine	0.005	0.995	0.000
Q43.2 Other congenital functional disorders of colon	0.005	0.995	0.000
Q43.1 Hirschsprung's disease	0.005	0.995	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.005	0.995	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.005	0.995	0.000
Q67 Congenital musculoskeletal deformities of head, face, spine and chest	0.005	0.995	0.000
Q43.8 Other specified congenital malformations of intestine	0.004	0.995	0.000
Q43.9 Congenital malformation of intestine, unspecified	0.004	0.995	0.000
Q99 Other chromosome abnormalities, not elsewhere classified	0.004	0.995	0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified	0.004	0.996	0.000
C67 Malignant neoplasm of bladder	0.000	0.996	0.004
C67.1 Dome of bladder	0.000	0.996	0.004
C67.8 Overlapping lesion of bladder	0.000	0.996	0.004
Q39.4 Oesophageal web	0.004	0.996	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.004	0.996	0.000
N14.4 Toxic nephropathy, not elsewhere classified	0.000	0.996	0.004
N14.3 Nephropathy induced by heavy metals	0.000	0.996	0.004
N14.2 Nephropathy induced by unspecified drug, medicament or biological substance	0.000	0.996	0.004
N14.0 Analgesic nephropathy	0.000	0.996	0.004
Q76.5 Cervical rib	0.004	0.996	0.000
N10 Acute tubulo-interstitial nephritis	0.000	0.996	0.004
N16.8 Renal tubulo-interstitial disorders in other diseases classified elsewhere	0.000	0.996	0.004
N16.5 Renal tubulo-interstitial disorders in transplant rejection	0.000	0.996	0.004
N16.4 Renal tubulo-interstitial disorders in systemic connective tissue disorders	0.000	0.996	0.004
N16.3 Renal tubulo-interstitial disorders in metabolic diseases	0.000	0.996	0.004
N16.2 Renal tubulo-interstitial disorders in blood diseases and disorders involving the immune mechanism	0.000	0.996	0.004
N16.1 Renal tubulo-interstitial disorders in neoplastic diseases	0.000	0.996	0.004
Q77 Osteochondrodysplasia with defects of growth of tubular bones and spine	0.004	0.996	0.000
Q67.5 Congenital deformity of spine	0.004	0.996	0.000
C67.4 Posterior wall of bladder	0.000	0.996	0.004
C67.0 Trigone of bladder	0.000	0.996	0.004
N15.1 Renal and perinephric abscess	0.000	0.996	0.004
Q66 Congenital deformities of feet	0.004	0.996	0.000
N15.8 Other specified renal tubulo-interstitial diseases	0.000	0.996	0.004
N15.0 Balkan nephropathy	0.000	0.996	0.004
D80.1 Nonfamilial hypogammaglobulinaemia	0.004	0.996	0.000
N11.9 Chronic tubulo-interstitial nephritis, unspecified	0.000	0.996	0.004
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified	0.004	0.996	0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified	0.004	0.996	0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified	0.004	0.996	0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified	0.004	0.996	0.000
Q91 Edwards' syndrome and Patau's syndrome	0.004	0.996	0.000
N11.8 Other chronic tubulo-interstitial nephritis	0.000	0.996	0.004
Q76.0 Spina bifida occulta	0.004	0.996	0.000
D80 Immunodeficiency with predominantly antibody defects	0.004	0.996	0.000
C67.3 Anterior wall of bladder	0.000	0.996	0.004
Q90 Down's syndrome	0.004	0.996	0.000
M48.54 Collapsed vertebra, not elsewhere classified (Thoracic region)	0.000	0.996	0.004
Q75 Other congenital malformations of skull and face bones	0.004	0.996	0.000
Q73 Reduction defects of unspecified limb	0.004	0.996	0.000
Q72 Reduction defects of lower limb	0.004	0.996	0.000
Q71 Reduction defects of upper limb	0.004	0.996	0.000
Q70 Syndactyly	0.004	0.996	0.000
Q69 Polydactyly	0.004	0.996	0.000
Q68 Other congenital musculoskeletal deformities	0.004	0.996	0.000
Q00-Q07 Congenital malformations of the nervous system	0.004	0.996	0.000
Q40.8 Other specified congenital malformations of upper alimentary tract	0.004	0.996	0.000
Q30 Congenital malformations of nose	0.004	0.996	0.000
Q96 Turner's syndrome	0.004	0.996	0.000
Q39.9 Congenital malformation of oesophagus, unspecified	0.004	0.996	0.000
Q39.8 Other congenital malformations of oesophagus	0.004	0.996	0.000
Q39.5 Congenital dilatation of oesophagus	0.004	0.996	0.000
Q39.3 Congenital stenosis and stricture of oesophagus	0.004	0.996	0.000
Q39.2 Congenital tracheooesophageal fistula without atresia	0.004	0.996	0.000
Q39.1 Atresia of oesophagus with tracheooesophageal fistula	0.004	0.996	0.000
Q39.0 Atresia of oesophagus without fistula	0.004	0.996	0.000
Q39.6 Diverticulum of oesophagus	0.004	0.996	0.000
C34.1 Upper lobe, bronchus or lung	0.000	0.996	0.004
Q38 Other congenital malformations of tongue, mouth and pharynx	0.004	0.996	0.000
K90.9 Intestinal malabsorption, unspecified	0.004	0.996	0.000
Q34 Other congenital malformations of respiratory system	0.004	0.996	0.000
Q33 Congenital malformations of lung	0.004	0.996	0.000
Q32 Congenital malformations of trachea and bronchus	0.004	0.996	0.000
Q31 Congenital malformations of larynx	0.004	0.996	0.000
N11.0 Nonobstructive reflux-associated chronic pyelonephritis	0.000	0.996	0.004
N14.1 Nephropathy induced by other drugs, medicaments and biological substances	0.000	0.996	0.004
Q99.8 Other specified chromosome abnormalities	0.004	0.996	0.000
Q74 Other congenital malformations of limb(s)	0.004	0.996	0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified	0.004	0.996	0.000
Q98.4 Klinefelter's syndrome, unspecified	0.004	0.996	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.004	0.996	0.000
C67.5 Bladder neck	0.000	0.996	0.004
N16.0 Renal tubulo-interstitial disorders in infectious and parasitic diseases classified elsewhere	0.000	0.996	0.003
Q45.8 Other specified congenital malformations of digestive system	0.004	0.996	0.000
D80.4 Selective deficiency of immunoglobulin M [IgM]	0.004	0.996	0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses	0.004	0.996	0.000
Q37 Cleft palate with cleft lip	0.004	0.996	0.000
Q36 Cleft lip	0.004	0.996	0.000
Q35 Cleft palate	0.004	0.996	0.000
Q80-Q89 Other congenital malformations	0.004	0.996	0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified	0.004	0.996	0.000
Q40.3 Congenital malformation of stomach, unspecified	0.004	0.996	0.000
Q40.1 Congenital hiatus hernia	0.004	0.996	0.000
Q40.0 Congenital hypertrophic pyloric stenosis	0.004	0.996	0.000
Q79 Congenital malformations of musculoskeletal system, not elsewhere classified	0.004	0.996	0.000
Q76.9 Congenital malformation of bony thorax, unspecified	0.004	0.996	0.000
Q76.8 Other congenital malformations of bony thorax	0.004	0.996	0.000
Q76.7 Congenital malformation of sternum	0.004	0.996	0.000
Q76.6 Other congenital malformations of ribs	0.004	0.996	0.000
Q76.3 Congenital scoliosis due to congenital bony malformation	0.004	0.996	0.000
Q76.2 Congenital spondylolisthesis	0.004	0.996	0.000
Q76.1 Klippel-Feil syndrome	0.004	0.996	0.000
Q45.9 Congenital malformation of digestive system, unspecified	0.003	0.996	0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct	0.003	0.996	0.000
Q45.2 Congenital pancreatic cyst	0.003	0.996	0.000
Q45.1 Annular pancreas	0.003	0.996	0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas	0.003	0.996	0.000
Q66.7 Pes cavus	0.004	0.996	0.000
C34.0 Main bronchus	0.000	0.996	0.004
C67.6 Ureteric orifice	0.000	0.996	0.004
Q66.2 Metatarsus varus	0.004	0.996	0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified	0.003	0.996	0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine	0.003	0.996	0.000
Q41.2 Congenital absence, atresia and stenosis of ileum	0.003	0.996	0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum	0.003	0.996	0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum	0.003	0.996	0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified	0.003	0.996	0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine	0.003	0.996	0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula	0.003	0.996	0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula	0.003	0.996	0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula	0.003	0.996	0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula	0.003	0.996	0.000
Q77.4 Achondroplasia	0.003	0.996	0.000
Q65 Congenital deformities of hip	0.003	0.996	0.000
K66.0 Peritoneal adhesions	0.000	0.996	0.004
N11.1 Chronic obstructive pyelonephritis	0.000	0.996	0.003
Q67.8 Other congenital deformities of chest	0.003	0.996	0.000
Q67.7 Pectus carinatum	0.003	0.996	0.000
Q67.3 Plagiocephaly	0.003	0.996	0.000
Q67.2 Dolichocephaly	0.003	0.996	0.000
Q67.1 Compression facies	0.003	0.996	0.000
Q67.0 Facial asymmetry	0.003	0.996	0.000
V23.4 Driver injured in traffic accident	0.000	0.996	0.004
Q40.2 Other specified congenital malformations of stomach	0.003	0.996	0.000
C44.1 Skin of eyelid, including canthus	0.000	0.996	0.004
Q66.9 Congenital deformity of feet, unspecified	0.003	0.996	0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified	0.003	0.996	0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype	0.003	0.996	0.000
Q98.7 Male with sex chromosome mosaicism	0.003	0.996	0.000
Q98.6 Male with structurally abnormal sex chromosome	0.003	0.996	0.000
Q98.5 Karyotype 47,XYY	0.003	0.996	0.000
Q98.3 Other male with 46,XX karyotype	0.003	0.996	0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype	0.003	0.996	0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes	0.003	0.996	0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY	0.003	0.996	0.000
Q99.9 Chromosomal abnormality, unspecified	0.003	0.996	0.000
Q99.2 Fragile X chromosome	0.003	0.996	0.000
Q99.1 46,XX true hermaphrodite	0.003	0.996	0.000
Q99.0 Chimera 46,XX/46,XY	0.003	0.996	0.000
C67.7 Urachus	0.000	0.997	0.003
Q66.3 Other congenital varus deformities of feet	0.003	0.997	0.000
Q67.4 Other congenital deformities of skull, face and jaw	0.003	0.997	0.000
Q76.4 Other congenital malformations of spine, not associated with scoliosis	0.003	0.997	0.000
Q44.7 Other congenital malformations of liver	0.003	0.997	0.000
Q44.5 Other congenital malformations of bile ducts	0.003	0.997	0.000
Q44.4 Choledochal cyst	0.003	0.997	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.003	0.997	0.000
Q44.2 Atresia of bile ducts	0.003	0.997	0.000
Q44.1 Other congenital malformations of gallbladder	0.003	0.997	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.003	0.997	0.000
Q78 Other osteochondrodysplasias	0.003	0.997	0.000
Q50-Q56 Congenital malformations of genital organs	0.003	0.997	0.000
Q67.6 Pectus excavatum	0.003	0.997	0.000
Q77.9 Osteochondrodysplasia with defects of growth of tubular bones and spine, unspecified	0.003	0.997	0.000
Q77.8 Other osteochondrodysplasia with defects of growth of tubular bones and spine	0.003	0.997	0.000
Q77.7 Spondyloepiphyseal dysplasia	0.003	0.997	0.000
Q77.6 Chondroectodermal dysplasia	0.003	0.997	0.000
Q77.5 Diastrophic dysplasia	0.003	0.997	0.000
Q77.3 Chondrodysplasia punctata	0.003	0.997	0.000
Q77.2 Short rib syndrome	0.003	0.997	0.000
Q77.1 Thanatophoric short stature	0.003	0.997	0.000
Q77.0 Achondrogenesis	0.003	0.997	0.000
D80.2 Selective deficiency of immunoglobulin A [IgA]	0.003	0.997	0.000
Q03 Congenital hydrocephalus	0.003	0.997	0.000
Q66.6 Other congenital valgus deformities of feet	0.003	0.997	0.000
Q66.5 Congenital pes planus	0.003	0.997	0.000
Q66.4 Talipes calcaneovalgus	0.003	0.997	0.000
Q66.1 Talipes calcaneovarus	0.003	0.997	0.000
Q66.0 Talipes equinovarus	0.003	0.997	0.000
N15.9 Renal tubulo-interstitial disease, unspecified	0.000	0.997	0.003
C34 Malignant neoplasm of bronchus and lung	0.000	0.997	0.003
Q30.3 Congenital perforated nasal septum	0.003	0.997	0.000
D80.8 Other immunodeficiencies with predominantly antibody defects	0.003	0.997	0.000
D80.7 Transient hypogammaglobulinaemia of infancy	0.003	0.997	0.000
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia	0.003	0.997	0.000
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]	0.003	0.997	0.000
D80.0 Hereditary hypogammaglobulinaemia	0.003	0.997	0.000
Q91.7 Patau's syndrome, unspecified	0.003	0.997	0.000
Q91.6 Trisomy 13, translocation	0.003	0.997	0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q91.4 Trisomy 13, meiotic nondisjunction	0.003	0.997	0.000
Q91.3 Edwards' syndrome, unspecified	0.003	0.997	0.000
Q91.2 Trisomy 18, translocation	0.003	0.997	0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q91.0 Trisomy 18, meiotic nondisjunction	0.003	0.997	0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified	0.003	0.997	0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes	0.003	0.997	0.000
Q92.7 Triploidy and polyploidy	0.003	0.997	0.000
Q92.6 Extra marker chromosomes	0.003	0.997	0.000
Q92.5 Duplications with other complex rearrangements	0.003	0.997	0.000
Q92.4 Duplications seen only at prometaphase	0.003	0.997	0.000
Q92.3 Minor partial trisomy	0.003	0.997	0.000
Q92.2 Major partial trisomy	0.003	0.997	0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction	0.003	0.997	0.000
Q93.9 Deletion from autosomes, unspecified	0.003	0.997	0.000
Q93.8 Other deletions from the autosomes	0.003	0.997	0.000
Q93.7 Deletions with other complex rearrangements	0.003	0.997	0.000
Q93.6 Deletions seen only at prometaphase	0.003	0.997	0.000
Q93.5 Other deletions of part of a chromosome	0.003	0.997	0.000
Q93.4 Deletion of short arm of chromosome 5	0.003	0.997	0.000
Q93.3 Deletion of short arm of chromosome 4	0.003	0.997	0.000
Q93.2 Chromosome replaced with ring or dicentric	0.003	0.997	0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction	0.003	0.997	0.000
Q95.9 Balanced rearrangement and structural marker, unspecified	0.003	0.997	0.000
Q95.8 Other balanced rearrangements and structural markers	0.003	0.997	0.000
Q95.5 Individuals with autosomal fragile site	0.003	0.997	0.000
Q95.4 Individuals with marker heterochromatin	0.003	0.997	0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual	0.003	0.997	0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual	0.003	0.997	0.000
Q95.1 Chromosome inversion in normal individual	0.003	0.997	0.000
Q95.0 Balanced translocation and insertion in normal individual	0.003	0.997	0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified	0.003	0.997	0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype	0.003	0.997	0.000
Q97.3 Female with 46,XY karyotype	0.003	0.997	0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes	0.003	0.997	0.000
Q97.1 Female with more than three X chromosomes	0.003	0.997	0.000
Q97.0 Karyotype 47,XXX	0.003	0.997	0.000
Q90.2 Trisomy 21, translocation	0.003	0.997	0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)	0.003	0.997	0.000
Q90.0 Trisomy 21, meiotic nondisjunction	0.003	0.997	0.000
Q68.8 Other specified congenital musculoskeletal deformities	0.003	0.997	0.000
Q68.5 Congenital bowing of long bones of leg, unspecified	0.003	0.997	0.000
Q68.4 Congenital bowing of tibia and fibula	0.003	0.997	0.000
Q68.3 Congenital bowing of femur	0.003	0.997	0.000
Q68.2 Congenital deformity of knee	0.003	0.997	0.000
Q68.1 Congenital deformity of hand	0.003	0.997	0.000
Q68.0 Congenital deformity of sternocleidomastoid muscle	0.003	0.997	0.000
Q69.9 Polydactyly, unspecified	0.003	0.997	0.000
Q69.2 Accessory toe(s)	0.003	0.997	0.000
Q69.1 Accessory thumb(s)	0.003	0.997	0.000
Q69.0 Accessory finger(s)	0.003	0.997	0.000
Q70.9 Syndactyly, unspecified	0.003	0.997	0.000
Q70.4 Polysyndactyly	0.003	0.997	0.000
Q70.3 Webbed toes	0.003	0.997	0.000
Q70.2 Fused toes	0.003	0.997	0.000
Q70.1 Webbed fingers	0.003	0.997	0.000
Q70.0 Fused fingers	0.003	0.997	0.000
Q71.9 Reduction defect of upper limb, unspecified	0.003	0.997	0.000
Q71.8 Other reduction defects of upper limb(s)	0.003	0.997	0.000
Q71.6 Lobster-claw hand	0.003	0.997	0.000
Q71.5 Longitudinal reduction defect of ulna	0.003	0.997	0.000
Q71.4 Longitudinal reduction defect of radius	0.003	0.997	0.000
Q71.3 Congenital absence of hand and finger(s)	0.003	0.997	0.000
Q71.2 Congenital absence of both forearm and hand	0.003	0.997	0.000
Q71.1 Congenital absence of upper arm and forearm with hand present	0.003	0.997	0.000
Q71.0 Congenital complete absence of upper limb(s)	0.003	0.997	0.000
Q72.9 Reduction defect of lower limb, unspecified	0.003	0.997	0.000
Q72.8 Other reduction defects of lower limb(s)	0.003	0.997	0.000
Q72.7 Split foot	0.003	0.997	0.000
Q72.6 Longitudinal reduction defect of fibula	0.003	0.997	0.000
Q72.5 Longitudinal reduction defect of tibia	0.003	0.997	0.000
Q72.4 Longitudinal reduction defect of femur	0.003	0.997	0.000
Q72.3 Congenital absence of foot and toe(s)	0.003	0.997	0.000
Q72.2 Congenital absence of both lower leg and foot	0.003	0.997	0.000
Q72.1 Congenital absence of thigh and lower leg with foot present	0.003	0.997	0.000
Q72.0 Congenital complete absence of lower limb(s)	0.003	0.997	0.000
Q73.8 Other reduction defects of unspecified limb(s)	0.003	0.997	0.000
Q73.1 Phocomelia, unspecified limb(s)	0.003	0.997	0.000
Q73.0 Congenital absence of unspecified limb(s)	0.003	0.997	0.000
Q74.1 Congenital malformation of knee	0.003	0.997	0.000
Q75.9 Congenital malformation of skull and face bones, unspecified	0.003	0.997	0.000
Q75.8 Other specified congenital malformations of skull and face bones	0.003	0.997	0.000
Q75.5 Oculomandibular dysostosis	0.003	0.997	0.000
Q75.4 Mandibulofacial dysostosis	0.003	0.997	0.000
Q75.3 Macrocephaly	0.003	0.997	0.000
Q75.2 Hypertelorism	0.003	0.997	0.000
Q75.1 Craniofacial dysostosis	0.003	0.997	0.000
Q75.0 Craniosynostosis	0.003	0.997	0.000
Q90.9 Down's syndrome, unspecified	0.003	0.997	0.000
Q06 Other congenital malformations of spinal cord	0.003	0.997	0.000
Q01 Encephalocele	0.003	0.997	0.000
Q00 Anencephaly and similar malformations	0.003	0.997	0.000
Q02 Microcephaly	0.003	0.997	0.000
Q30.9 Congenital malformation of nose, unspecified	0.003	0.997	0.000
Q30.8 Other congenital malformations of nose	0.003	0.997	0.000
Q30.2 Fissured, notched and cleft nose	0.003	0.997	0.000
Q30.1 Agenesis and underdevelopment of nose	0.003	0.997	0.000
Q30.0 Choanal atresia	0.003	0.997	0.000
Q96.8 Other variants of Turner's syndrome	0.003	0.997	0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome	0.003	0.997	0.000
Q96.3 Mosaicism, 45,X/46,XX or XY	0.003	0.997	0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)	0.003	0.997	0.000
Q96.1 Karyotype 46,X iso (Xq)	0.003	0.997	0.000
Q96.0 Karyotype 45,X	0.003	0.997	0.000
Q85 Phakomatoses, not elsewhere classified	0.003	0.997	0.000
I70.20 Atherosclerosis of arteries of extremities (without gangrene)	0.003	0.997	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.003	0.997	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.003	0.997	0.000
Q31.9 Congenital malformation of larynx, unspecified	0.003	0.997	0.000
Q31.8 Other congenital malformations of larynx	0.003	0.997	0.000
Q31.5 Congenital laryngomalacia	0.003	0.997	0.000
Q31.4 Congenital laryngeal stridor	0.003	0.997	0.000
Q31.3 Laryngocele	0.003	0.997	0.000
Q31.2 Laryngeal hypoplasia	0.003	0.997	0.000
Q31.1 Congenital subglottic stenosis	0.003	0.997	0.000
Q31.0 Web of larynx	0.003	0.997	0.000
Q32.4 Other congenital malformations of bronchus	0.003	0.997	0.000
Q32.3 Congenital stenosis of bronchus	0.003	0.997	0.000
Q32.2 Congenital bronchomalacia	0.003	0.997	0.000
Q32.1 Other congenital malformations of trachea	0.003	0.997	0.000
Q32.0 Congenital tracheomalacia	0.003	0.997	0.000
Q33.9 Congenital malformation of lung, unspecified	0.003	0.997	0.000
Q33.8 Other congenital malformations of lung	0.003	0.997	0.000
Q33.6 Hypoplasia and dysplasia of lung	0.003	0.997	0.000
Q33.5 Ectopic tissue in lung	0.003	0.997	0.000
Q33.4 Congenital bronchiectasis	0.003	0.997	0.000
Q33.3 Agenesis of lung	0.003	0.997	0.000
Q33.2 Sequestration of lung	0.003	0.997	0.000
Q33.1 Accessory lobe of lung	0.003	0.997	0.000
Q33.0 Congenital cystic lung	0.003	0.997	0.000
Q34.9 Congenital malformation of respiratory system, unspecified	0.003	0.997	0.000
Q34.8 Other specified congenital malformations of respiratory system	0.003	0.997	0.000

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

The full results table can be downloaded from this page.

The TreeWAS Database is the result of research conducted at the Oxford Big Data Institute at the University of Oxford.

This research has been conducted using the UK Biobank Resource (application number 10625). This work uses data provided by patients and collected by the NHS as part of their care and support.

This research has been conducted with the support of the Wellcome Trust (100956/Z/13/Z and 090532/Z/09/Z and 100308/Z/12/Z), the Danish National Research Foundation, Takeda, the Medical Research Council (MC_UU_12010/3), the Oak Foundation (OCAY-15-520), the National Institute for Health Research (NIHR) Oxford Biomedical Research Centre (BRC), the Wellcome Trust/Royal Society (204290/Z/16/Z) and the Li Ka Shing Foundation.

Variant-specific associations