TreeWAS – Variant ID: rs7916852

Hospitalization Episode Statistics (HES)

Self-Reported Statistics (SRS)

Hierarchical visualisation How to interpret this figure?

Click here to show this figure without filtering.

Click on a node to zoom (except terminal nodes).

Download this figure in format

Results table

Term	Risk posterior probability	No effect posterior probability	Protective posterior probability
J06.9 Acute upper respiratory infection, unspecified	0.018	0.982	0.000
F31 Bipolar affective disorder	0.000	0.982	0.018
F31.0 Bipolar affective disorder, current episode hypomanic	0.000	0.983	0.017
F30-F39 Mood [affective] disorders	0.000	0.983	0.017
F32 Depressive episode	0.000	0.983	0.017
F33 Recurrent depressive disorder	0.000	0.983	0.017
F31.9 Bipolar affective disorder, unspecified	0.000	0.984	0.016
F33.1 Recurrent depressive disorder, current episode moderate	0.000	0.984	0.016
F32.9 Depressive episode, unspecified	0.000	0.984	0.016
F31.2 Bipolar affective disorder, current episode manic with psychotic symptoms	0.000	0.985	0.015
F31.6 Bipolar affective disorder, current episode mixed	0.000	0.986	0.014
F32.0 Mild depressive episode	0.000	0.986	0.014
F33.3 Recurrent depressive disorder, current episode severe with psychotic symptoms	0.000	0.986	0.014
F32.1 Moderate depressive episode	0.000	0.986	0.014
F32.3 Severe depressive episode with psychotic symptoms	0.000	0.987	0.013
F31.7 Bipolar affective disorder, currently in remission	0.000	0.987	0.013
F33.0 Recurrent depressive disorder, current episode mild	0.000	0.987	0.013
F31.5 Bipolar affective disorder, current episode severe depression with psychotic symptoms	0.000	0.987	0.013
F33.9 Recurrent depressive disorder, unspecified	0.000	0.987	0.013
F38 Other mood [affective] disorders	0.000	0.987	0.012
F30 Manic episode	0.000	0.987	0.012
F32.8 Other depressive episodes	0.000	0.988	0.012
F31.3 Bipolar affective disorder, current episode mild or moderate depression	0.000	0.988	0.012
F33.8 Other recurrent depressive disorders	0.000	0.988	0.012
F33.4 Recurrent depressive disorder, currently in remission	0.000	0.988	0.012
F31.1 Bipolar affective disorder, current episode manic without psychotic symptoms	0.000	0.988	0.012
F39 Unspecified mood [affective] disorder	0.000	0.988	0.012
F34 Persistent mood [affective] disorders	0.000	0.988	0.012
J06 Acute upper respiratory infections of multiple and unspecified sites	0.012	0.988	0.000
F31.8 Other bipolar affective disorders	0.000	0.989	0.011
F31.4 Bipolar affective disorder, current episode severe depression without psychotic symptoms	0.000	0.989	0.011
G40.3 Generalised idiopathic epilepsy and epileptic syndromes	0.000	0.989	0.011
F30.9 Manic episode, unspecified	0.000	0.989	0.011
F33.2 Recurrent depressive disorder, current episode severe without psychotic symptoms	0.000	0.990	0.010
F32.2 Severe depressive episode without psychotic symptoms	0.000	0.990	0.010
H33.2 Serous retinal detachment	0.000	0.991	0.009
F38.8 Other specified mood [affective] disorders	0.000	0.991	0.009
F38.1 Other recurrent mood [affective] disorders	0.000	0.991	0.009
F38.0 Other single mood [affective] disorders	0.000	0.991	0.009
F30.8 Other manic episodes	0.000	0.991	0.009
F30.2 Mania with psychotic symptoms	0.000	0.991	0.009
I51.7 Cardiomegaly	0.009	0.991	0.000
F34.9 Persistent mood [affective] disorder, unspecified	0.000	0.991	0.009
F34.8 Other persistent mood [affective] disorders	0.000	0.991	0.009
F34.0 Cyclothymia	0.000	0.991	0.009
G40 Epilepsy	0.000	0.991	0.009
J06.8 Other acute upper respiratory infections of multiple sites	0.008	0.991	0.000
J06.0 Acute laryngopharyngitis	0.008	0.991	0.000
F30.0 Hypomania	0.000	0.992	0.008
Z30.1 Insertion of (intra-uterine) contraceptive device	0.008	0.992	0.000
F34.1 Dysthymia	0.000	0.992	0.008
G40.1 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures	0.000	0.992	0.008
F30.1 Mania without psychotic symptoms	0.000	0.992	0.007
G40.8 Other epilepsy	0.000	0.992	0.008
N92.6 Irregular menstruation, unspecified	0.008	0.992	0.000
H33.1 Retinoschisis and retinal cysts	0.000	0.992	0.007
H33 Retinal detachments and breaks	0.000	0.992	0.008
G40.9 Epilepsy, unspecified	0.000	0.993	0.007
G40.7 Petit mal, unspecified, without grand mal seizures	0.000	0.993	0.007
N30.3 Trigonitis	0.007	0.993	0.000
J40 Bronchitis, not specified as acute or chronic	0.000	0.993	0.007
J00-J06 Acute upper respiratory infections	0.007	0.993	0.000
H33.4 Traction detachment of retina	0.000	0.993	0.007
G40.4 Other generalised epilepsy and epileptic syndromes	0.000	0.994	0.006
Z83.3 Family history of diabetes mellitus	0.000	0.994	0.006
H33.3 Retinal breaks without detachment	0.000	0.994	0.006
J04 Acute laryngitis and tracheitis	0.006	0.994	0.000
G40.5 Special epileptic syndromes	0.000	0.994	0.006
N28.9 Disorder of kidney and ureter, unspecified	0.006	0.994	0.000
G40.6 Grand mal seizures, unspecified (with or without petit mal)	0.000	0.994	0.006
N28.1 Cyst of kidney, acquired	0.006	0.994	0.000
G40.0 Localisation-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localised onset	0.000	0.994	0.006
J02 Acute pharyngitis	0.006	0.994	0.000
Z83.5 Family history of eye and ear disorders	0.000	0.994	0.006
H33.5 Other retinal detachments	0.000	0.994	0.006
J04.0 Acute laryngitis	0.006	0.994	0.000
J02.9 Acute pharyngitis, unspecified	0.006	0.994	0.000
J01 Acute sinusitis	0.005	0.995	0.000
G40.2 Localisation-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures	0.000	0.995	0.005
Z83 Family history of other specific disorders	0.000	0.995	0.005
J04.1 Acute tracheitis	0.005	0.995	0.000
J05 Acute obstructive laryngitis [croup] and epiglottitis	0.005	0.995	0.000
Z83.4 Family history of other endocrine, nutritional and metabolic diseases	0.000	0.995	0.005
J01.0 Acute maxillary sinusitis	0.005	0.995	0.000
J04.2 Acute laryngotracheitis	0.005	0.995	0.000
N28 Other disorders of kidney and ureter, not elsewhere classified	0.005	0.995	0.000
J02.8 Acute pharyngitis due to other specified organisms	0.004	0.995	0.000
J02.0 Streptococcal pharyngitis	0.004	0.995	0.000
Z83.2 Family history of diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism	0.000	0.996	0.004
Z83.6 Family history of diseases of the respiratory system	0.000	0.996	0.004
J05.1 Acute epiglottitis	0.004	0.996	0.000
J01.8 Other acute sinusitis	0.004	0.996	0.000
J01.4 Acute pansinusitis	0.004	0.996	0.000
J01.3 Acute sphenoidal sinusitis	0.004	0.996	0.000
J01.2 Acute ethmoidal sinusitis	0.004	0.996	0.000
J01.1 Acute frontal sinusitis	0.004	0.996	0.000
Z83.0 Family history of human immunodeficiency virus [HIV]	0.000	0.996	0.004
J05.0 Acute obstructive laryngitis [croup]	0.004	0.996	0.000
Z83.1 Family history of other infectious and parasitic diseases	0.000	0.996	0.004
J03 Acute tonsillitis	0.004	0.996	0.000
J01.9 Acute sinusitis, unspecified	0.003	0.996	0.000
T18.1 Foreign body in oesophagus	0.000	0.997	0.003
S80.9 Superficial injury of lower leg, unspecified	0.003	0.997	0.000
H53.8 Other visual disturbances	0.003	0.997	0.000
B97.8 Other viral agents as the cause of diseases classified to other chapters	0.003	0.997	0.000
G35 Multiple sclerosis	0.000	0.997	0.003
J00 Acute nasopharyngitis [common cold]	0.003	0.997	0.000
I51 Complications and ill-defined descriptions of heart disease	0.003	0.997	0.000
Q07.0 Arnold-Chiari syndrome	0.003	0.997	0.000
B97.7 Papillomavirus as the cause of diseases classified to other chapters	0.003	0.997	0.000
I51.8 Other ill-defined heart diseases	0.003	0.997	0.000
H53.0 Amblyopia ex anopsia	0.003	0.997	0.000
J03.8 Acute tonsillitis due to other specified organisms	0.003	0.997	0.000
J03.0 Streptococcal tonsillitis	0.003	0.997	0.000
H53 Visual disturbances	0.003	0.997	0.000
F03 Unspecified dementia	0.000	0.997	0.003
N28.0 Ischaemia and infarction of kidney	0.003	0.997	0.000
B97 Viral agents as the cause of diseases classified to other chapters	0.003	0.997	0.000
D26.1 Corpus uteri	0.003	0.997	0.000
I51.6 Cardiovascular disease, unspecified	0.003	0.997	0.000
I51.1 Rupture of chordae tendineae, not elsewhere classified	0.003	0.997	0.000
Q61.3 Polycystic kidney, unspecified	0.003	0.997	0.000
H18.4 Corneal degeneration	0.003	0.997	0.000
H33.0 Retinal detachment with retinal break	0.000	0.997	0.003
B97.4 Respiratory synctial virus as the cause of diseases classified to other chapters	0.003	0.997	0.000
T18 Foreign body in alimentary tract	0.000	0.997	0.003
G83.4 Cauda equina syndrome	0.000	0.997	0.003
I51.5 Myocardial degeneration	0.002	0.997	0.000
I51.2 Rupture of papillary muscle, not elsewhere classified	0.002	0.997	0.000
H53.2 Diplopia	0.003	0.997	0.000
Q61 Cystic kidney disease	0.003	0.997	0.000
B96.3 Haemophilus influenzae [H. influenzae] as the cause of diseases classified to other chapters	0.000	0.997	0.003
H53.1 Subjective visual disturbances	0.002	0.997	0.000
S42.20 Fracture of upper end of humerus (closed)	0.002	0.998	0.000
C50.5 Lower-outer quadrant of breast	0.002	0.998	0.000
Q07 Other congenital malformations of nervous system	0.002	0.998	0.000
N28.8 Other specified disorders of kidney and ureter	0.002	0.998	0.000
R82.9 Other and unspecified abnormal finding in urine	0.000	0.998	0.002
T18.5 Foreign body in anus and rectum	0.000	0.998	0.002
H53.6 Night blindness	0.002	0.998	0.000
H53.5 Colour vision deficiencies	0.002	0.998	0.000
H53.3 Other disorders of binocular vision	0.002	0.998	0.000
I51.0 Cardiac septal defect, acquired	0.002	0.998	0.000
Q63 Other congenital malformations of kidney	0.002	0.998	0.000
I51.3 Intracardiac thrombosis, not elsewhere classified	0.002	0.998	0.000
Q63.2 Ectopic kidney	0.002	0.998	0.000
Q61.0 Congenital single renal cyst	0.002	0.998	0.000
Z83.7 Family history of diseases of the digestive system	0.000	0.998	0.002
Q60-Q64 Congenital malformations of the urinary system	0.002	0.998	0.000
B97.6 Parvovirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
B97.5 Reovirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
B97.3 Retrovirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
B97.2 Coronavirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
B97.1 Enterovirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
B97.0 Adenovirus as the cause of diseases classified to other chapters	0.002	0.998	0.000
Q63.1 Lobulated, fused and horseshoe kidney	0.002	0.998	0.000
H53.4 Visual field defects	0.002	0.998	0.000
T18.8 Foreign body in other and multiple parts of alimentary tract	0.000	0.998	0.002
T18.4 Foreign body in colon	0.000	0.998	0.002
T18.3 Foreign body in small intestine	0.000	0.998	0.002
T18.2 Foreign body in stomach	0.000	0.998	0.002
T18.0 Foreign body in mouth	0.000	0.998	0.002
T18.9 Foreign body in alimentary tract, part unspecified	0.000	0.998	0.002
H18.1 Bullous keratopathy	0.002	0.998	0.000
Q61.9 Cystic kidney disease, unspecified	0.002	0.998	0.000
Q61.8 Other cystic kidney diseases	0.002	0.998	0.000
Q61.5 Medullary cystic kidney	0.002	0.998	0.000
Q61.4 Renal dysplasia	0.002	0.998	0.000
Q61.1 Polycystic kidney, infantile type	0.002	0.998	0.000
D10.1 Tongue	0.002	0.998	0.000
H18 Other disorders of cornea	0.002	0.998	0.000
G30.9 Alzheimer's disease, unspecified	0.000	0.998	0.002
Q07.9 Congenital malformation of nervous system, unspecified	0.002	0.998	0.000
Q07.8 Other specified congenital malformations of nervous system	0.002	0.998	0.000
B96.4 Proteus (mirabilis)(morganii) as the cause of diseases classified to other chapters	0.000	0.998	0.002
I51.4 Myocarditis, unspecified	0.002	0.998	0.000
Q61.2 Polycystic kidney, adult type	0.002	0.998	0.000
Q87.4 Marfan's syndrome	0.002	0.998	0.000
H18.8 Other specified disorders of cornea	0.002	0.998	0.000
O35.1 Maternal care for (suspected) chromosomal abnormality in foetus	0.000	0.998	0.002
Q63.9 Congenital malformation of kidney, unspecified	0.002	0.998	0.000
Q63.8 Other specified congenital malformations of kidney	0.002	0.998	0.000
Q63.3 Hyperplastic and giant kidney	0.002	0.998	0.000
H54.4 Blindness, one eye	0.002	0.998	0.000
Q64 Other congenital malformations of urinary system	0.002	0.998	0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter	0.002	0.998	0.000
D63.8 Anaemia in other chronic diseases classified elsewhere	0.002	0.998	0.000
O69.2 Labour and delivery complicated by other cord entanglement	0.002	0.998	0.000
Q00-Q07 Congenital malformations of the nervous system	0.002	0.998	0.000
H18.0 Corneal pigmentations and deposits	0.002	0.998	0.000
Q63.0 Accessory kidney	0.002	0.998	0.000
Q44.6 Cystic disease of liver	0.002	0.998	0.000
Q85.0 Neurofibromatosis (nonmalignant)	0.002	0.998	0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems	0.002	0.998	0.000
D41.0 Kidney	0.002	0.998	0.000
I51.9 Heart disease, unspecified	0.002	0.998	0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver	0.002	0.998	0.000
G83 Other paralytic syndromes	0.000	0.998	0.002
H54 Blindness and low vision	0.002	0.998	0.000
Q85 Phakomatoses, not elsewhere classified	0.002	0.998	0.000
Q80-Q89 Other congenital malformations	0.002	0.998	0.000
M48.07 Spinal stenosis (Lumbosacral region)	0.000	0.998	0.002
M77.91 Enthesopathy, unspecified (Shoulder region)	0.002	0.998	0.000
M86.97 Osteomyelitis, unspecified (Ankle and foot)	0.002	0.998	0.000
H18.7 Other corneal deformities	0.002	0.998	0.000
H18.6 Keratoconus	0.002	0.998	0.000
H18.3 Changes in corneal membranes	0.002	0.998	0.000
Q44.5 Other congenital malformations of bile ducts	0.002	0.998	0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck	0.002	0.998	0.000
S06.00 Concussion (without open intracranial wound)	0.002	0.998	0.000
H18.2 Other corneal oedema	0.002	0.998	0.000
H54.7 Unspecified visual loss	0.002	0.998	0.000
K50.1 Crohn's disease of large intestine	0.002	0.998	0.000
Q11.1 Other anophthalmos	0.002	0.998	0.000
H53-H54 Visual disturbances and blindness	0.002	0.998	0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos	0.002	0.998	0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities	0.002	0.998	0.000
B96.1 Klebsiella pneumoniae [K. pneumoniae] as the cause of diseases classified to other chapters	0.000	0.998	0.002
Z35.2 Supervision of pregnancy with other poor reproductive or obstetric history	0.000	0.998	0.002
N25-N29 Other disorders of kidney and ureter	0.002	0.998	0.000
S32.10 Fracture of sacrum (closed)	0.000	0.998	0.002
G55.8 Nerve root and plexus compressions in other diseases classified elsewhere	0.000	0.998	0.002
Y45.3 Other nonsteroidal anti-inflammatory drugs [NSAID]	0.000	0.998	0.002
G83.9 Paralytic syndrome, unspecified	0.000	0.998	0.002
O35.8 Maternal care for other (suspected) foetal abnormality and damage	0.000	0.998	0.002
Q62.5 Duplication of ureter	0.002	0.998	0.000
F00-F09 Organic, including symptomatic, mental disorders	0.000	0.998	0.002
Q64.3 Other atresia and stenosis of urethra and bladder neck	0.001	0.998	0.000
T17.2 Foreign body in pharynx	0.000	0.998	0.002
G35-G37 Demyelinating diseases of the central nervous system	0.000	0.998	0.002
G83.8 Other specified paralytic syndromes	0.000	0.998	0.002
Q62.8 Other congenital malformations of ureter	0.001	0.998	0.000
Q62.7 Congenital vesico-uretero-renal reflux	0.001	0.998	0.000
Q62.6 Malposition of ureter	0.001	0.998	0.000
Q62.4 Agenesis of ureter	0.001	0.998	0.000
Q62.3 Other obstructive defects of renal pelvis and ureter	0.001	0.998	0.000
Q62.2 Congenital megaloureter	0.001	0.998	0.000
Q62.1 Atresia and stenosis of ureter	0.001	0.998	0.000
Q62.0 Congenital hydronephrosis	0.001	0.998	0.000
Q64.9 Congenital malformation of urinary system, unspecified	0.001	0.998	0.000
Q64.8 Other specified congenital malformations of urinary system	0.001	0.998	0.000
Q64.7 Other congenital malformations of bladder and urethra	0.001	0.998	0.000
Q64.6 Congenital diverticulum of bladder	0.001	0.998	0.000
Q64.5 Congenital absence of bladder and urethra	0.001	0.998	0.000
Q64.4 Malformation of urachus	0.001	0.998	0.000
Q64.2 Congenital posterior urethral valves	0.001	0.998	0.000
Q64.1 Exstrophy of urinary bladder	0.001	0.998	0.000
Q64.0 Epispadias	0.001	0.998	0.000
Q06 Other congenital malformations of spinal cord	0.001	0.998	0.000
Q04 Other congenital malformations of brain	0.001	0.998	0.000
Q03 Congenital hydrocephalus	0.001	0.998	0.000
Q01 Encephalocele	0.001	0.998	0.000
Q00 Anencephaly and similar malformations	0.001	0.998	0.000
Q02 Microcephaly	0.001	0.998	0.000
Q60 Renal agenesis and other reduction defects of kidney	0.001	0.998	0.000
M00.97 Pyogenic arthritis, unspecified (Ankle and foot)	0.002	0.998	0.000
F00.9 Dementia in Alzheimer's disease, unspecified	0.000	0.998	0.002
O35.9 Maternal care for (suspected) foetal abnormality and damage, unspecified	0.000	0.998	0.002
N25 Disorders resulting from impaired renal tubular function	0.002	0.998	0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit	0.002	0.998	0.000
H53.9 Visual disturbance, unspecified	0.002	0.998	0.000
S42.2 Fracture of upper end of humerus	0.002	0.998	0.000
Q15 Other congenital malformations of eye	0.001	0.998	0.000
T17 Foreign body in respiratory tract	0.000	0.998	0.002
Q38-Q45 Other congenital malformations of the digestive system	0.002	0.998	0.000
N25.8 Other disorders resulting from impaired renal tubular function	0.001	0.998	0.000
Q85.8 Other phakomatoses, not elsewhere classified	0.001	0.998	0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified	0.001	0.998	0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes	0.001	0.998	0.000
Q87.3 Congenital malformation syndromes involving early overgrowth	0.001	0.998	0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs	0.001	0.998	0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature	0.001	0.998	0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance	0.001	0.998	0.000
O35 Maternal care for known or suspected foetal abnormality and damage	0.000	0.998	0.002
Q17 Other congenital malformations of ear	0.001	0.998	0.000
N92.4 Excessive bleeding in the premenopausal period	0.002	0.998	0.000
M47.12 Other spondylosis with myelopathy (Cervical region)	0.002	0.998	0.000
S32.40 Fracture of acetabulum (closed)	0.000	0.998	0.002
H18.5 Hereditary corneal dystrophies	0.002	0.998	0.000
H54.1 Blindness, one eye, low vision, other eye	0.001	0.998	0.000
Q44.7 Other congenital malformations of liver	0.001	0.998	0.000
Q44.4 Choledochal cyst	0.001	0.998	0.000
Q44.3 Congenital stenosis and stricture of bile ducts	0.001	0.998	0.000
Q44.2 Atresia of bile ducts	0.001	0.998	0.000
Q44.1 Other congenital malformations of gallbladder	0.001	0.998	0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder	0.001	0.998	0.000
G83.5 Locked-in syndrome	0.000	0.998	0.001
G83.3 Monoplegia, unspecified	0.000	0.998	0.001
G83.0 Diplegia of upper limbs	0.000	0.998	0.001
H18.9 Disorder of cornea, unspecified	0.001	0.998	0.000
H54.6 Unqualified visual loss, one eye	0.001	0.998	0.000
H54.5 Low vision, one eye	0.001	0.998	0.000
H54.3 Unqualified visual loss, both eyes	0.001	0.998	0.000
H54.2 Low vision, both eyes	0.001	0.998	0.000
Q85.1 Tuberous sclerosis	0.001	0.998	0.000
F00 Dementia in Alzheimer's disease	0.000	0.998	0.002
M00.90 Pyogenic arthritis, unspecified (Multiple sites)	0.001	0.998	0.000
Q10.0 Congenital ptosis	0.001	0.998	0.000
Y45.1 Salicylates	0.000	0.998	0.002
Z71.9 Counselling, unspecified	0.000	0.998	0.002
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified	0.001	0.998	0.000
Q84 Other congenital malformations of integument	0.001	0.998	0.000
Q81 Epidermolysis bullosa	0.001	0.998	0.000
Q80 Congenital ichthyosis	0.001	0.998	0.000
T15-T19 Effects of foreign body entering through natural orifice	0.000	0.998	0.002
M00.92 Pyogenic arthritis, unspecified (Upper arm)	0.001	0.998	0.000
M48.06 Spinal stenosis (Lumbar region)	0.000	0.998	0.002
I71.0 Dissection of aorta [any part]	0.002	0.998	0.000
K29.0 Acute haemorrhagic gastritis	0.002	0.998	0.000
Q16 Congenital malformations of ear causing impairment of hearing	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
Q83 Congenital malformations of breast	0.001	0.998	0.000
S42.80 Fracture of other parts of shoulder and upper arm (closed)	0.001	0.998	0.000
M00.9 Pyogenic arthritis, unspecified	0.001	0.998	0.000
Q11.3 Macrophthalmos	0.001	0.998	0.000
Q11.2 Microphthalmos	0.001	0.998	0.000
Q11.0 Cystic eyeball	0.001	0.998	0.000
Q15.0 Congenital glaucoma	0.001	0.998	0.000
T17.9 Foreign body in respiratory tract, part unspecified	0.000	0.998	0.001
F06 Other mental disorders due to brain damage and dysfunction and to physical disease	0.000	0.998	0.001
N30 Cystitis	0.002	0.998	0.000
Q89 Other congenital malformations, not elsewhere classified	0.001	0.998	0.000
Q35-Q37 Cleft lip and cleft palate	0.001	0.998	0.000
Q30-Q34 Congenital malformations of the respiratory system	0.001	0.998	0.000
B96 Other bacterial agents as the cause of diseases classified to other chapters	0.000	0.998	0.002
G37 Other demyelinating diseases of central nervous system	0.000	0.998	0.001
N29 Other disorders of kidney and ureter in diseases classified elsewhere	0.001	0.998	0.000
N27 Small kidney of unknown cause	0.001	0.998	0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified	0.001	0.998	0.000
M89.04 Algoneurodystrophy (Hand)	0.001	0.998	0.000
S02.00 Fracture of vault of skull (closed)	0.001	0.998	0.000
H31.8 Other specified disorders of choroid	0.000	0.998	0.001
J03.9 Acute tonsillitis, unspecified	0.001	0.998	0.000
Q17.5 Prominent ear	0.001	0.998	0.000
F09 Unspecified organic or symptomatic mental disorder	0.000	0.998	0.001
F04 Organic amnesic syndrome, not induced by alcohol and other psychoactive substances	0.000	0.998	0.001
Q85.9 Phakomatosis, unspecified	0.001	0.999	0.000
S32.1 Fracture of sacrum	0.000	0.999	0.001
G36 Other acute disseminated demyelination	0.000	0.999	0.001
Q45 Other congenital malformations of digestive system	0.001	0.999	0.000
M89.03 Algoneurodystrophy (Forearm)	0.001	0.999	0.000
S32.70 Multiple fractures of lumbar spine and pelvis (closed)	0.000	0.999	0.001
B25.9 Cytomegaloviral disease, unspecified	0.001	0.999	0.000
G55.3 Nerve root and plexus compressions in other dorsopathies	0.000	0.999	0.001
G55.2 Nerve root and plexus compressions in spondylosis	0.000	0.999	0.001
G83.2 Monoplegia of upper limb	0.000	0.999	0.001
J93.1 Other spontaneous pneumothorax	0.001	0.999	0.000
N25.9 Disorder resulting from impaired renal tubular function, unspecified	0.001	0.999	0.000
N25.1 Nephrogenic diabetes insipidus	0.001	0.999	0.000
N25.0 Renal osteodystrophy	0.001	0.999	0.000
Q00.2 Iniencephaly	0.001	0.999	0.000
Q00.1 Craniorachischisis	0.001	0.999	0.000
Q00.0 Anencephaly	0.001	0.999	0.000
Q01.9 Encephalocele, unspecified	0.001	0.999	0.000
Q01.8 Encephalocele of other sites	0.001	0.999	0.000
Q01.2 Occipital encephalocele	0.001	0.999	0.000
Q01.1 Nasofrontal encephalocele	0.001	0.999	0.000
Q01.0 Frontal encephalocele	0.001	0.999	0.000
Q03.9 Congenital hydrocephalus, unspecified	0.001	0.999	0.000
Q03.8 Other congenital hydrocephalus	0.001	0.999	0.000
Q03.1 Atresia of foramina of Magendie and Luschka	0.001	0.999	0.000
Q03.0 Malformations of aqueduct of Sylvius	0.001	0.999	0.000
Q04.9 Congenital malformation of brain, unspecified	0.001	0.999	0.000
Q04.8 Other specified congenital malformations of brain	0.001	0.999	0.000
Q04.6 Congenital cerebral cysts	0.001	0.999	0.000
Q04.5 Megalencephaly	0.001	0.999	0.000
Q04.4 Septo-optic dysplasia	0.001	0.999	0.000
Q04.3 Other reduction deformities of brain	0.001	0.999	0.000
Q04.2 Holoprosencephaly	0.001	0.999	0.000
Q04.1 Arhinencephaly	0.001	0.999	0.000
Q04.0 Congenital malformations of corpus callosum	0.001	0.999	0.000
Q06.9 Congenital malformation of spinal cord, unspecified	0.001	0.999	0.000
Q06.8 Other specified congenital malformations of spinal cord	0.001	0.999	0.000
Q06.4 Hydromyelia	0.001	0.999	0.000
Q06.3 Other congenital cauda equina malformations	0.001	0.999	0.000
Q06.2 Diastematomyelia	0.001	0.999	0.000
Q06.1 Hypoplasia and dysplasia of spinal cord	0.001	0.999	0.000
Q06.0 Amyelia	0.001	0.999	0.000
Q60.6 Potter's syndrome	0.001	0.999	0.000
Q60.5 Renal hypoplasia, unspecified	0.001	0.999	0.000
Q60.4 Renal hypoplasia, bilateral	0.001	0.999	0.000
Q60.3 Renal hypoplasia, unilateral	0.001	0.999	0.000
Q60.2 Renal agenesis, unspecified	0.001	0.999	0.000
Q60.1 Renal agenesis, bilateral	0.001	0.999	0.000
R50.8 Other specified fever	0.001	0.999	0.000
S42.21 Fracture of upper end of humerus (open)	0.001	0.999	0.000
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
Q10.5 Congenital stenosis and stricture of lachrymal duct	0.001	0.999	0.000
Q10.4 Absence and agenesis of lachrymal apparatus	0.001	0.999	0.000
Q10.3 Other congenital malformations of eyelid	0.001	0.999	0.000
Q10.2 Congenital entropion	0.001	0.999	0.000
Q10.1 Congenital ectropion	0.001	0.999	0.000
Q15.9 Congenital malformation of eye, unspecified	0.001	0.999	0.000
Q15.8 Other specified congenital malformations of eye	0.001	0.999	0.000
T17.5 Foreign body in bronchus	0.000	0.999	0.001
T17.4 Foreign body in trachea	0.000	0.999	0.001
T17.3 Foreign body in larynx	0.000	0.999	0.001
T17.1 Foreign body in nostril	0.000	0.999	0.001
T17.0 Foreign body in nasal sinus	0.000	0.999	0.001
F07 Personality and behavioural disorders due to brain disease, damage and dysfunction	0.000	0.999	0.001
Q18 Other congenital malformations of face and neck	0.001	0.999	0.000
Q12 Congenital lens malformations	0.001	0.999	0.000
Q42 Congenital absence, atresia and stenosis of large intestine	0.001	0.999	0.000
Q41 Congenital absence, atresia and stenosis of small intestine	0.001	0.999	0.000
Q40 Other congenital malformations of upper alimentary tract	0.001	0.999	0.000
Q38 Other congenital malformations of tongue, mouth and pharynx	0.001	0.999	0.000
C85.9 Non-Hodgkin's lymphoma, unspecified type	0.001	0.999	0.000
G83.1 Monoplegia of lower limb	0.000	0.999	0.001
O35.7 Maternal care for (suspected) damage to foetus by other medical procedures	0.000	0.999	0.001
O35.6 Maternal care for (suspected) damage to foetus by radiation	0.000	0.999	0.001
O35.5 Maternal care for (suspected) damage to foetus by drugs	0.000	0.999	0.001
O35.4 Maternal care for (suspected) damage to foetus from alcohol	0.000	0.999	0.001
O35.3 Maternal care for (suspected) damage to foetus from viral disease in mother	0.000	0.999	0.001
O35.2 Maternal care for (suspected) hereditary disease in foetus	0.000	0.999	0.001
O35.0 Maternal care for (suspected) central nervous system malformation in foetus	0.000	0.999	0.001
Q17.9 Congenital malformation of ear, unspecified	0.001	0.999	0.000
Q17.8 Other specified congenital malformations of ear	0.001	0.999	0.000
Q17.4 Misplaced ear	0.001	0.999	0.000
Q17.3 Other misshapen ear	0.001	0.999	0.000
Q17.2 Microtia	0.001	0.999	0.000
Q17.1 Macrotia	0.001	0.999	0.000
Q17.0 Accessory auricle	0.001	0.999	0.000
G82.1 Spastic paraplegia	0.000	0.999	0.001
I31.3 Pericardial effusion (noninflammatory)	0.000	0.999	0.001
S32.4 Fracture of acetabulum	0.000	0.999	0.001
F00.1 Dementia in Alzheimer's disease with late onset	0.000	0.999	0.001
G37.9 Demyelinating disease of central nervous system, unspecified	0.000	0.999	0.001
Q05 Spina bifida	0.001	0.999	0.000
T19 Foreign body in genito-urinary tract	0.000	0.999	0.001
T15 Foreign body on external eye	0.000	0.999	0.001
T16 Foreign body in ear	0.000	0.999	0.001
E28.2 Polycystic ovarian syndrome	0.000	0.999	0.001
G55.0 Nerve root and plexus compressions in neoplastic disease	0.000	0.999	0.001
G82.5 Tetraplegia, unspecified	0.000	0.999	0.001
Q13.9 Congenital malformation of anterior segment of eye, unspecified	0.001	0.999	0.000
Q13.8 Other congenital malformations of anterior segment of eye	0.001	0.999	0.000
Q13.5 Blue sclera	0.001	0.999	0.000
Q13.4 Other congenital corneal malformations	0.001	0.999	0.000
Q13.3 Congenital corneal opacity	0.001	0.999	0.000
Q13.2 Other congenital malformations of iris	0.001	0.999	0.000
Q13.1 Absence of iris	0.001	0.999	0.000
Q13.0 Coloboma of iris	0.001	0.999	0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified	0.001	0.999	0.000
Q14.8 Other congenital malformations of posterior segment of eye	0.001	0.999	0.000
Q14.3 Congenital malformation of choroid	0.001	0.999	0.000
Q14.2 Congenital malformation of optic disk	0.001	0.999	0.000
Q14.1 Congenital malformation of retina	0.001	0.999	0.000
Q14.0 Congenital malformation of vitreous humour	0.001	0.999	0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified	0.001	0.999	0.000
Q16.5 Congenital malformation of inner ear	0.001	0.999	0.000
Q16.4 Other congenital malformations of middle ear	0.001	0.999	0.000
Q16.3 Congenital malformation of ear ossicles	0.001	0.999	0.000
Q16.2 Absence of eustachian tube	0.001	0.999	0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)	0.001	0.999	0.000
Q16.0 Congenital absence of (ear) auricle	0.001	0.999	0.000
Q80.9 Congenital ichthyosis, unspecified	0.001	0.999	0.000
Q80.8 Other congenital ichthyosis	0.001	0.999	0.000
Q80.4 Harlequin foetus	0.001	0.999	0.000
Q80.3 Congenital bullous ichthyosiform erythroderma	0.001	0.999	0.000
Q80.2 Lamellar ichthyosis	0.001	0.999	0.000
Q80.1 X-linked ichthyosis	0.001	0.999	0.000
Q80.0 Ichthyosis vulgaris	0.001	0.999	0.000
Q81.9 Epidermolysis bullosa, unspecified	0.001	0.999	0.000
Q81.8 Other epidermolysis bullosa	0.001	0.999	0.000
Q81.2 Epidermolysis bullosa dystrophica	0.001	0.999	0.000
Q81.1 Epidermolysis bullosa letalis	0.001	0.999	0.000
Q81.0 Epidermolysis bullosa simplex	0.001	0.999	0.000
Q83.8 Other congenital malformations of breast	0.001	0.999	0.000
Q84.9 Congenital malformation of integument, unspecified	0.001	0.999	0.000
Q84.8 Other specified congenital malformations of integument	0.001	0.999	0.000
Q84.6 Other congenital malformations of nails	0.001	0.999	0.000
Q84.5 Enlarged and hypertrophic nails	0.001	0.999	0.000
Q84.4 Congenital leukonychia	0.001	0.999	0.000
Q84.3 Anonychia	0.001	0.999	0.000
Q84.2 Other congenital malformations of hair	0.001	0.999	0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified	0.001	0.999	0.000
Q84.0 Congenital alopecia	0.001	0.999	0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes	0.001	0.999	0.000
Q86.2 Dysmorphism due to warfarin	0.001	0.999	0.000
Q86.1 Foetal hydantoin syndrome	0.001	0.999	0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)	0.001	0.999	0.000
F02 Dementia in other diseases classified elsewhere	0.000	0.999	0.001
M00.99 Pyogenic arthritis, unspecified (Site unspecified)	0.001	0.999	0.000
M00.98 Pyogenic arthritis, unspecified (Other)	0.001	0.999	0.000
M00.95 Pyogenic arthritis, unspecified (Pelvic region and thigh)	0.001	0.999	0.000
M00.94 Pyogenic arthritis, unspecified (Hand)	0.001	0.999	0.000
M00.93 Pyogenic arthritis, unspecified (Forearm)	0.001	0.999	0.000
M77.96 Enthesopathy, unspecified (Lower leg)	0.001	0.999	0.000
D26.0 Cervix uteri	0.001	0.999	0.000
F00.2 Dementia in Alzheimer's disease, atypical or mixed type	0.000	0.999	0.001
F06.9 Unspecified mental disorder due to brain damage and dysfunction and to physical disease	0.000	0.999	0.001
F06.8 Other specified mental disorders due to brain damage and dysfunction and to physical disease	0.000	0.999	0.001
F06.7 Mild cognitive disorder	0.000	0.999	0.001
F06.6 Organic emotionally labile [asthenic] disorder	0.000	0.999	0.001
F06.5 Organic dissociative disorder	0.000	0.999	0.001
F06.4 Organic anxiety disorder	0.000	0.999	0.001
F06.3 Organic mood [affective] disorders	0.000	0.999	0.001
F06.2 Organic delusional [schizophrenia-like] disorder	0.000	0.999	0.001

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