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Variant-specific associations

rs17377726
log Bayes Factor = <0.0001
Chromosome 3   position 78,896,235  (GRCh37) Explore rs17377726 on Ensembl!
Variant rs17377726 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
 
Z91.0 Personal history of allergy, other than to drugs and biological substances
0.025 0.975 0.000
Z91.6 Personal history of other physical trauma
0.022 0.978 0.000
Z91 Personal history of risk-factors, not elsewhere classified
0.022 0.978 0.000
Z91.1 Personal history of noncompliance with medical treatment and regimen
0.020 0.980 0.000
Z91.8 Personal history of other specified risk-factors, not elsewhere classified
0.016 0.983 0.000
Z91.7 Personal history of female genital mutilation
0.016 0.984 0.000
Z91.4 Personal history of psychological trauma, not elsewhere classified
0.016 0.984 0.000
Z91.3 Personal history of unhealthy sleep-wake schedule
0.016 0.984 0.000
Z91.2 Personal history of poor personal hygiene
0.016 0.984 0.000
Z91.5 Personal history of self-harm
0.012 0.988 0.000
Z41.1 Other plastic surgery for unacceptable cosmetic appearance
0.011 0.989 0.000
K82 Other diseases of gallbladder
0.011 0.989 0.000
K82.4 Cholesterolosis of gallbladder
0.011 0.989 0.000
K82.1 Hydrops of gallbladder
0.010 0.989 0.000
K82.9 Disease of gallbladder, unspecified
0.010 0.990 0.000
K82.8 Other specified diseases of gallbladder
0.009 0.991 0.000
K82.2 Perforation of gallbladder
0.009 0.991 0.000
K82.3 Fistula of gallbladder
0.008 0.992 0.000
K82.0 Obstruction of gallbladder
0.008 0.992 0.000
Z36.8 Other antenatal screening
0.007 0.993 0.000
R29.6 Tendency to fall, not elsewhere classified
0.007 0.993 0.000
Z36.3 Antenatal screening for malformations using ultrasound and other physical methods
0.006 0.994 0.000
Z36 Antenatal screening
0.006 0.994 0.000
Z41 Procedures for purposes other than remedying health state
0.006 0.994 0.000
G62.9 Polyneuropathy, unspecified
0.006 0.994 0.000
Z41.8 Other procedures for purposes other than remedying health state
0.005 0.995 0.000
Z36.0 Antenatal screening for chromosomal anomalies
0.005 0.995 0.000
Z51.4 Preparatory care for treatment, not elsewhere classified
0.000 0.995 0.005
Z36.2 Other antenatal screening based on amniocentesis
0.005 0.995 0.000
Z36.4 Antenatal screening for foetal growth retardation using ultrasound and other physical methods
0.005 0.995 0.000
Z36.1 Antenatal screening for raised alphafetoprotein level
0.005 0.995 0.000
Z36.5 Antenatal screening for isoimmunisation
0.005 0.995 0.000
Z41.9 Procedures for purposes other than remedying health state, unspecified
0.004 0.995 0.000
Z41.3 Ear piercing
0.004 0.995 0.000
Z41.2 Routine and ritual circumcision
0.004 0.995 0.000
Z41.0 Hair transplant
0.004 0.995 0.000
G62 Other polyneuropathies
0.005 0.995 0.000
G62.8 Other specified polyneuropathies
0.005 0.995 0.000
Z36.9 Antenatal screening, unspecified
0.004 0.996 0.000
D86.9 Sarcoidosis, unspecified
0.004 0.996 0.000
R47.0 Dysphasia and aphasia
0.004 0.996 0.000
O80.9 Single spontaneous delivery, unspecified
0.004 0.996 0.000
Z51.0 Radiotherapy session
0.000 0.996 0.004
K80.2 Calculus of gallbladder without cholecystitis
0.000 0.996 0.004
G62.2 Polyneuropathy due to other toxic agents
0.003 0.996 0.000
G62.1 Alcoholic polyneuropathy
0.003 0.996 0.000
M10.99 Gout, unspecified (Site unspecified)
0.004 0.996 0.000
D86 Sarcoidosis
0.003 0.997 0.000
Q82.8 Other specified congenital malformations of skin
0.003 0.997 0.000
K83.0 Cholangitis
0.003 0.997 0.000
Q82 Other congenital malformations of skin
0.003 0.997 0.000
D86.0 Sarcoidosis of lung
0.003 0.997 0.000
Q80-Q89 Other congenital malformations
0.003 0.997 0.000
Z51.3 Blood transfusion without reported diagnosis
0.000 0.997 0.003
Q60-Q64 Congenital malformations of the urinary system
0.003 0.997 0.000
Q63.0 Accessory kidney
0.003 0.997 0.000
Q63 Other congenital malformations of kidney
0.003 0.997 0.000
G62.0 Drug-induced polyneuropathy
0.003 0.997 0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.003 0.997 0.000
K80-K87 Disorders of gallbladder, biliary tract and pancreas
0.003 0.997 0.000
Z88.6 Personal history of allergy to analgesic agent
0.003 0.997 0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.003 0.997 0.000
Z51 Other medical care
0.000 0.997 0.003
Q00-Q07 Congenital malformations of the nervous system
0.003 0.997 0.000
H66.9 Otitis media, unspecified
0.000 0.997 0.003
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit
0.003 0.997 0.000
Q89 Other congenital malformations, not elsewhere classified
0.003 0.997 0.000
E05.9 Thyrotoxicosis, unspecified
0.000 0.997 0.003
Q61 Cystic kidney disease
0.003 0.997 0.000
D86.8 Sarcoidosis of other and combined sites
0.003 0.997 0.000
Q10.0 Congenital ptosis
0.003 0.997 0.000
E05.0 Thyrotoxicosis with diffuse goitre
0.000 0.997 0.003
Q82.5 Congenital nonneoplastic naevus
0.003 0.997 0.000
Q04 Other congenital malformations of brain
0.003 0.997 0.000
Q12 Congenital lens malformations
0.003 0.997 0.000
Q83 Congenital malformations of breast
0.003 0.997 0.000
Q05 Spina bifida
0.003 0.997 0.000
D86.3 Sarcoidosis of skin
0.003 0.997 0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.003 0.997 0.000
D86.1 Sarcoidosis of lymph nodes
0.003 0.997 0.000
H21.5 Other adhesions and disruptions of iris and ciliary body
0.003 0.997 0.000
N32.9 Bladder disorder, unspecified
0.003 0.997 0.000
Q60 Renal agenesis and other reduction defects of kidney
0.003 0.997 0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.003 0.997 0.000
Z86.1 Personal history of infectious and parasitic diseases
0.000 0.997 0.003
Q18 Other congenital malformations of face and neck
0.003 0.997 0.000
Q85 Phakomatoses, not elsewhere classified
0.003 0.997 0.000
Q82.9 Congenital malformation of skin, unspecified
0.002 0.997 0.000
Q82.4 Ectodermal dysplasia (anhidrotic)
0.002 0.997 0.000
Q82.3 Incontinentia pigmenti
0.002 0.997 0.000
Q82.2 Mastocytosis
0.002 0.997 0.000
Q82.1 Xeroderma pigmentosum
0.002 0.997 0.000
Q82.0 Hereditary lymphoedema
0.002 0.997 0.000
K83 Other diseases of biliary tract
0.003 0.997 0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
0.003 0.997 0.000
Q84 Other congenital malformations of integument
0.003 0.997 0.000
Q81 Epidermolysis bullosa
0.003 0.997 0.000
Q80 Congenital ichthyosis
0.003 0.997 0.000
R47 Speech disturbances, not elsewhere classified
0.003 0.997 0.000
K86 Other diseases of pancreas
0.003 0.997 0.000
R26.8 Other and unspecified abnormalities of gait and mobility
0.003 0.997 0.000
Q28.2 Arteriovenous malformation of cerebral vessels
0.003 0.997 0.000
Q61.3 Polycystic kidney, unspecified
0.003 0.997 0.000
Q64 Other congenital malformations of urinary system
0.002 0.997 0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
0.002 0.997 0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems
0.002 0.997 0.000
Q04.6 Congenital cerebral cysts
0.002 0.997 0.000
Z51.5 Palliative care
0.000 0.997 0.003
Q89.2 Congenital malformations of other endocrine glands
0.002 0.997 0.000
O63.1 Prolonged second stage (of labour)
0.003 0.997 0.000
Q63.9 Congenital malformation of kidney, unspecified
0.002 0.997 0.000
Q63.8 Other specified congenital malformations of kidney
0.002 0.997 0.000
Q63.3 Hyperplastic and giant kidney
0.002 0.997 0.000
Q63.2 Ectopic kidney
0.002 0.997 0.000
Q63.1 Lobulated, fused and horseshoe kidney
0.002 0.997 0.000
Q05.9 Spina bifida, unspecified
0.002 0.997 0.000
Q17 Other congenital malformations of ear
0.002 0.997 0.000
Q16 Congenital malformations of ear causing impairment of hearing
0.002 0.997 0.000
Q15 Other congenital malformations of eye
0.002 0.997 0.000
Q14 Congenital malformations of posterior segment of eye
0.002 0.997 0.000
Q13 Congenital malformations of anterior segment of eye
0.002 0.997 0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos
0.002 0.997 0.000
Q28 Other congenital malformations of circulatory system
0.002 0.997 0.000
Q20-Q28 Congenital malformations of the circulatory system
0.002 0.997 0.000
Q18.1 Preauricular sinus and cyst
0.002 0.997 0.000
K87 Disorders of gallbladder, biliary tract and pancreas in diseases classified elsewhere
0.002 0.997 0.000
K86.2 Cyst of pancreas
0.002 0.997 0.000
Q12.0 Congenital cataract
0.002 0.997 0.000
Q38-Q45 Other congenital malformations of the digestive system
0.002 0.997 0.000
Q35-Q37 Cleft lip and cleft palate
0.002 0.997 0.000
Q30-Q34 Congenital malformations of the respiratory system
0.002 0.997 0.000
M10.9 Gout, unspecified
0.002 0.997 0.000
R47.1 Dysarthria and anarthria
0.002 0.997 0.000
F41.0 Panic disorder [episodic paroxysmal anxiety]
0.000 0.997 0.002
F80.1 Expressive language disorder
0.002 0.997 0.000
H74.4 Polyp of middle ear
0.000 0.997 0.002
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
0.002 0.998 0.000
Z51.6 Desensitisation to allergens
0.000 0.998 0.002
H66 Suppurative and unspecified otitis media
0.000 0.998 0.002
Q06 Other congenital malformations of spinal cord
0.002 0.998 0.000
Q03 Congenital hydrocephalus
0.002 0.998 0.000
Q01 Encephalocele
0.002 0.998 0.000
Q00 Anencephaly and similar malformations
0.002 0.998 0.000
Q02 Microcephaly
0.002 0.998 0.000
F40.2 Specific (isolated) phobias
0.000 0.998 0.002
Q07 Other congenital malformations of nervous system
0.002 0.998 0.000
Q10.7 Congenital malformation of orbit
0.002 0.998 0.000
Q10.6 Other congenital malformations of lachrymal apparatus
0.002 0.998 0.000
Q10.5 Congenital stenosis and stricture of lachrymal duct
0.002 0.998 0.000
Q10.4 Absence and agenesis of lachrymal apparatus
0.002 0.998 0.000
Q10.3 Other congenital malformations of eyelid
0.002 0.998 0.000
Q10.2 Congenital entropion
0.002 0.998 0.000
Q10.1 Congenital ectropion
0.002 0.998 0.000
Q85.8 Other phakomatoses, not elsewhere classified
0.002 0.998 0.000
N23 Unspecified renal colic
0.000 0.998 0.002
Q61.0 Congenital single renal cyst
0.002 0.998 0.000
Q83.1 Accessory breast
0.002 0.998 0.000
Q89.9 Congenital malformation, unspecified
0.002 0.998 0.000
Q89.8 Other specified congenital malformations
0.002 0.998 0.000
Q89.7 Multiple congenital malformations, not elsewhere classified
0.002 0.998 0.000
Q89.4 Conjoined twins
0.002 0.998 0.000
Q89.3 Situs inversus
0.002 0.998 0.000
Q89.1 Congenital malformations of adrenal gland
0.002 0.998 0.000
Q89.0 Congenital malformations of spleen
0.002 0.998 0.000
N50.8 Other specified disorders of male genital organs
0.002 0.998 0.000
Q60.0 Renal agenesis, unilateral
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
H21 Other disorders of iris and ciliary body
0.002 0.998 0.000
Q27 Other congenital malformations of peripheral vascular system
0.002 0.998 0.000
G60-G64 Polyneuropathies and other disorders of the peripheral nervous system
0.002 0.998 0.000
Q98.4 Klinefelter's syndrome, unspecified
0.002 0.998 0.000
E05 Thyrotoxicosis [hyperthyroidism]
0.000 0.998 0.002
K85 Acute pancreatitis
0.002 0.998 0.000
H21.0 Hyphaema
0.002 0.998 0.000
K86.0 Alcohol-induced chronic pancreatitis
0.002 0.998 0.000
Q12.9 Congenital lens malformation, unspecified
0.002 0.998 0.000
Q12.8 Other congenital lens malformations
0.002 0.998 0.000
Q12.4 Spherophakia
0.002 0.998 0.000
Q12.3 Congenital aphakia
0.002 0.998 0.000
Q12.2 Coloboma of lens
0.002 0.998 0.000
Q12.1 Congenital displaced lens
0.002 0.998 0.000
M10.97 Gout, unspecified (Ankle and foot)
0.002 0.998 0.000
H11.3 Conjunctival haemorrhage
0.002 0.998 0.000
K86.3 Pseudocyst of pancreas
0.002 0.998 0.000
Q04.9 Congenital malformation of brain, unspecified
0.002 0.998 0.000
Q04.8 Other specified congenital malformations of brain
0.002 0.998 0.000
Q04.5 Megalencephaly
0.002 0.998 0.000
Q04.4 Septo-optic dysplasia
0.002 0.998 0.000
Q04.3 Other reduction deformities of brain
0.002 0.998 0.000
Q04.2 Holoprosencephaly
0.002 0.998 0.000
Q04.1 Arhinencephaly
0.002 0.998 0.000
Q04.0 Congenital malformations of corpus callosum
0.002 0.998 0.000
Q05.8 Sacral spina bifida without hydrocephalus
0.002 0.998 0.000
Q05.7 Lumbar spina bifida without hydrocephalus
0.002 0.998 0.000
Q05.6 Thoracic spina bifida without hydrocephalus
0.002 0.998 0.000
Q05.5 Cervical spina bifida without hydrocephalus
0.002 0.998 0.000
Q05.4 Unspecified spina bifida with hydrocephalus
0.002 0.998 0.000
Q05.3 Sacral spina bifida with hydrocephalus
0.002 0.998 0.000
Q05.2 Lumbar spina bifida with hydrocephalus
0.002 0.998 0.000
Q05.1 Thoracic spina bifida with hydrocephalus
0.002 0.998 0.000
Q05.0 Cervical spina bifida with hydrocephalus
0.002 0.998 0.000
Q83.9 Congenital malformation of breast, unspecified
0.002 0.998 0.000
Q83.8 Other congenital malformations of breast
0.002 0.998 0.000
Q83.3 Accessory nipple
0.002 0.998 0.000
Q83.2 Absent nipple
0.002 0.998 0.000
Q83.0 Congenital absence of breast with absent nipple
0.002 0.998 0.000
H74 Other disorders of middle ear and mastoid
0.000 0.998 0.002
H18.2 Other corneal oedema
0.002 0.998 0.000
Q60.6 Potter's syndrome
0.002 0.998 0.000
Q60.5 Renal hypoplasia, unspecified
0.002 0.998 0.000
Q60.4 Renal hypoplasia, bilateral
0.002 0.998 0.000
Q60.3 Renal hypoplasia, unilateral
0.002 0.998 0.000
Q60.2 Renal agenesis, unspecified
0.002 0.998 0.000
Q60.1 Renal agenesis, bilateral
0.002 0.998 0.000
Q99 Other chromosome abnormalities, not elsewhere classified
0.002 0.998 0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified
0.002 0.998 0.000
Q96 Turner's syndrome
0.002 0.998 0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified
0.002 0.998 0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified
0.002 0.998 0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
0.002 0.998 0.000
Q91 Edwards' syndrome and Patau's syndrome
0.002 0.998 0.000
Q90 Down's syndrome
0.002 0.998 0.000
K86.9 Disease of pancreas, unspecified
0.002 0.998 0.000
Q18.9 Congenital malformation of face and neck, unspecified
0.002 0.998 0.000
Q18.8 Other specified congenital malformations of face and neck
0.002 0.998 0.000
Q18.7 Microcheilia
0.002 0.998 0.000
Q18.6 Macrocheilia
0.002 0.998 0.000
Q18.5 Microstomia
0.002 0.998 0.000
Q18.4 Macrostomia
0.002 0.998 0.000
Q18.3 Webbing of neck
0.002 0.998 0.000
Q18.2 Other branchial cleft malformations
0.002 0.998 0.000
Q85.9 Phakomatosis, unspecified
0.002 0.998 0.000
Q85.1 Tuberous sclerosis
0.002 0.998 0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.002 0.998 0.000
Q61.2 Polycystic kidney, adult type
0.002 0.998 0.000
Q80.9 Congenital ichthyosis, unspecified
0.002 0.998 0.000
Q80.8 Other congenital ichthyosis
0.002 0.998 0.000
Q80.4 Harlequin foetus
0.002 0.998 0.000
Q80.3 Congenital bullous ichthyosiform erythroderma
0.002 0.998 0.000
Q80.2 Lamellar ichthyosis
0.002 0.998 0.000
Q80.1 X-linked ichthyosis
0.002 0.998 0.000
Q80.0 Ichthyosis vulgaris
0.002 0.998 0.000
Q81.9 Epidermolysis bullosa, unspecified
0.002 0.998 0.000
Q81.8 Other epidermolysis bullosa
0.002 0.998 0.000
Q81.2 Epidermolysis bullosa dystrophica
0.002 0.998 0.000
Q81.1 Epidermolysis bullosa letalis
0.002 0.998 0.000
Q81.0 Epidermolysis bullosa simplex
0.002 0.998 0.000
Q84.9 Congenital malformation of integument, unspecified
0.002 0.998 0.000
Q84.8 Other specified congenital malformations of integument
0.002 0.998 0.000
Q84.6 Other congenital malformations of nails
0.002 0.998 0.000
Q84.5 Enlarged and hypertrophic nails
0.002 0.998 0.000
Q84.4 Congenital leukonychia
0.002 0.998 0.000
Q84.3 Anonychia
0.002 0.998 0.000
Q84.2 Other congenital malformations of hair
0.002 0.998 0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified
0.002 0.998 0.000
Q84.0 Congenital alopecia
0.002 0.998 0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes
0.002 0.998 0.000
Q86.2 Dysmorphism due to warfarin
0.002 0.998 0.000
Q86.1 Foetal hydantoin syndrome
0.002 0.998 0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)
0.002 0.998 0.000
D80.1 Nonfamilial hypogammaglobulinaemia
0.002 0.998 0.000
K83.5 Biliary cyst
0.002 0.998 0.000
K83.4 Spasm of sphincter of Oddi
0.002 0.998 0.000
K83.3 Fistula of bile duct
0.002 0.998 0.000
K83.2 Perforation of bile duct
0.002 0.998 0.000
Z51.8 Other specified medical care
0.000 0.998 0.002
M10.90 Gout, unspecified (Multiple sites)
0.002 0.998 0.000
D23.3 Skin of other and unspecified parts of face
0.002 0.998 0.000
Q62.8 Other congenital malformations of ureter
0.002 0.998 0.000
Q62.7 Congenital vesico-uretero-renal reflux
0.002 0.998 0.000
Q62.6 Malposition of ureter
0.002 0.998 0.000
Q62.5 Duplication of ureter
0.002 0.998 0.000
Q62.4 Agenesis of ureter
0.002 0.998 0.000
Q62.3 Other obstructive defects of renal pelvis and ureter
0.002 0.998 0.000
Q62.2 Congenital megaloureter
0.002 0.998 0.000
Q62.1 Atresia and stenosis of ureter
0.002 0.998 0.000
Q62.0 Congenital hydronephrosis
0.002 0.998 0.000
Q64.9 Congenital malformation of urinary system, unspecified
0.002 0.998 0.000
Q64.8 Other specified congenital malformations of urinary system
0.002 0.998 0.000
Q64.7 Other congenital malformations of bladder and urethra
0.002 0.998 0.000
Q64.6 Congenital diverticulum of bladder
0.002 0.998 0.000
Q64.5 Congenital absence of bladder and urethra
0.002 0.998 0.000
Q64.4 Malformation of urachus
0.002 0.998 0.000
Q64.3 Other atresia and stenosis of urethra and bladder neck
0.002 0.998 0.000
Q64.2 Congenital posterior urethral valves
0.002 0.998 0.000
Q64.1 Exstrophy of urinary bladder
0.002 0.998 0.000
Q64.0 Epispadias
0.002 0.998 0.000
Q38 Other congenital malformations of tongue, mouth and pharynx
0.002 0.998 0.000
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
0.002 0.998 0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes
0.002 0.998 0.000
Q87.3 Congenital malformation syndromes involving early overgrowth
0.002 0.998 0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs
0.002 0.998 0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature
0.002 0.998 0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
0.002 0.998 0.000
Q27.8 Other specified congenital malformations of peripheral vascular system
0.002 0.998 0.000
R47.8 Other and unspecified speech disturbances
0.002 0.998 0.000
D23.9 Skin, unspecified
0.002 0.998 0.000
H72.9 Perforation of tympanic membrane, unspecified
0.000 0.998 0.002
Q11.3 Macrophthalmos
0.002 0.998 0.000
Q11.2 Microphthalmos
0.002 0.998 0.000
Q11.1 Other anophthalmos
0.002 0.998 0.000
Q11.0 Cystic eyeball
0.002 0.998 0.000
Q13.9 Congenital malformation of anterior segment of eye, unspecified
0.002 0.998 0.000
Q13.8 Other congenital malformations of anterior segment of eye
0.002 0.998 0.000
Q13.5 Blue sclera
0.002 0.998 0.000
Q13.4 Other congenital corneal malformations
0.002 0.998 0.000
Q13.3 Congenital corneal opacity
0.002 0.998 0.000
Q13.2 Other congenital malformations of iris
0.002 0.998 0.000
Q13.1 Absence of iris
0.002 0.998 0.000
Q13.0 Coloboma of iris
0.002 0.998 0.000
Q14.9 Congenital malformation of posterior segment of eye, unspecified
0.002 0.998 0.000
Q14.8 Other congenital malformations of posterior segment of eye
0.002 0.998 0.000
Q14.3 Congenital malformation of choroid
0.002 0.998 0.000
Q14.2 Congenital malformation of optic disk
0.002 0.998 0.000
Q14.1 Congenital malformation of retina
0.002 0.998 0.000
Q14.0 Congenital malformation of vitreous humour
0.002 0.998 0.000
Q15.9 Congenital malformation of eye, unspecified
0.002 0.998 0.000
Q15.8 Other specified congenital malformations of eye
0.002 0.998 0.000
Q15.0 Congenital glaucoma
0.002 0.998 0.000
Q16.9 Congenital malformation of ear causing impairment of hearing, unspecified
0.002 0.998 0.000
Q16.5 Congenital malformation of inner ear
0.002 0.998 0.000
Q16.4 Other congenital malformations of middle ear
0.002 0.998 0.000
Q16.3 Congenital malformation of ear ossicles
0.002 0.998 0.000
Q16.2 Absence of eustachian tube
0.002 0.998 0.000
Q16.1 Congenital absence, atresia and stricture of auditory canal (external)
0.002 0.998 0.000
Q16.0 Congenital absence of (ear) auricle
0.002 0.998 0.000
Q17.9 Congenital malformation of ear, unspecified
0.002 0.998 0.000
Q17.8 Other specified congenital malformations of ear
0.002 0.998 0.000
Q17.5 Prominent ear
0.002 0.998 0.000
Q17.4 Misplaced ear
0.002 0.998 0.000
Q17.3 Other misshapen ear
0.002 0.998 0.000
Q17.2 Microtia
0.002 0.998 0.000
Q17.1 Macrotia
0.002 0.998 0.000
Q17.0 Accessory auricle
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
Q28.3 Other malformations of cerebral vessels
0.002 0.998 0.000
Q28.1 Other malformations of precerebral vessels
0.002 0.998 0.000
Q28.0 Arteriovenous malformation of precerebral vessels
0.002 0.998 0.000
Q87.4 Marfan's syndrome
0.002 0.998 0.000
H72 Perforation of tympanic membrane
0.000 0.998 0.002
Q26 Congenital malformations of great veins
0.002 0.998 0.000
Q25 Congenital malformations of great arteries
0.002 0.998 0.000
Q24 Other congenital malformations of heart
0.002 0.998 0.000
Q22 Congenital malformations of pulmonary and tricuspid valves
0.002 0.998 0.000
Q20 Congenital malformations of cardiac chambers and connexions
0.002 0.998 0.000
H65-H75 Diseases of middle ear and mastoid
0.000 0.998 0.002
K87.1 Disorders of pancreas in diseases classified elsewhere
0.002 0.998 0.000
K87.0 Disorders of gallbladder and biliary tract in diseases classified elsewhere
0.002 0.998 0.000
Q34 Other congenital malformations of respiratory system
0.002 0.998 0.000
Q33 Congenital malformations of lung
0.002 0.998 0.000
Q32 Congenital malformations of trachea and bronchus
0.002 0.998 0.000
Q31 Congenital malformations of larynx
0.002 0.998 0.000
Q30 Congenital malformations of nose
0.002 0.998 0.000
Q37 Cleft palate with cleft lip
0.002 0.998 0.000
Q36 Cleft lip
0.002 0.998 0.000
Q35 Cleft palate
0.002 0.998 0.000
Q45 Other congenital malformations of digestive system
0.002 0.998 0.000
Q42 Congenital absence, atresia and stenosis of large intestine
0.002 0.998 0.000
Q41 Congenital absence, atresia and stenosis of small intestine
0.002 0.998 0.000
Q40 Other congenital malformations of upper alimentary tract
0.002 0.998 0.000
Q39 Congenital malformations of oesophagus
0.002 0.998 0.000
Q50-Q56 Congenital malformations of genital organs
0.002 0.998 0.000
M10.98 Gout, unspecified (Other)
0.002 0.998 0.000
M10.95 Gout, unspecified (Pelvic region and thigh)
0.002 0.998 0.000
M10.94 Gout, unspecified (Hand)
0.002 0.998 0.000
M10.93 Gout, unspecified (Forearm)
0.002 0.998 0.000
M10.92 Gout, unspecified (Upper arm)
0.002 0.998 0.000
M10.91 Gout, unspecified (Shoulder region)
0.002 0.998 0.000
G61 Inflammatory polyneuropathy
0.002 0.998 0.000
Q43 Other congenital malformations of intestine
0.002 0.998 0.000
H18 Other disorders of cornea
0.002 0.998 0.000
H66.4 Suppurative otitis media, unspecified
0.000 0.998 0.002
H66.2 Chronic atticoantral suppurative otitis media
0.000 0.998 0.002
H66.1 Chronic tubotympanic suppurative otitis media
0.000 0.998 0.002
H66.0 Acute suppurative otitis media
0.000 0.998 0.002
K85.9 Acute pancreatitis, unspecified
0.002 0.998 0.000
Q00.2 Iniencephaly
0.002 0.998 0.000
Q00.1 Craniorachischisis
0.002 0.998 0.000
Q00.0 Anencephaly
0.002 0.998 0.000
Q01.9 Encephalocele, unspecified
0.002 0.998 0.000
Q01.8 Encephalocele of other sites
0.002 0.998 0.000
Q01.2 Occipital encephalocele
0.002 0.998 0.000
Q01.1 Nasofrontal encephalocele
0.002 0.998 0.000
Q01.0 Frontal encephalocele
0.002 0.998 0.000
Q03.9 Congenital hydrocephalus, unspecified
0.002 0.998 0.000
Q03.8 Other congenital hydrocephalus
0.002 0.998 0.000
Q03.1 Atresia of foramina of Magendie and Luschka
0.002 0.998 0.000
Q03.0 Malformations of aqueduct of Sylvius
0.002 0.998 0.000
Q06.9 Congenital malformation of spinal cord, unspecified
0.002 0.998 0.000
Q06.8 Other specified congenital malformations of spinal cord
0.002 0.998 0.000
Q06.4 Hydromyelia
0.002 0.998 0.000
Q06.3 Other congenital cauda equina malformations
0.002 0.998 0.000
Q06.2 Diastematomyelia
0.002 0.998 0.000
Q06.1 Hypoplasia and dysplasia of spinal cord
0.002 0.998 0.000
Q06.0 Amyelia
0.002 0.998 0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified
0.002 0.998 0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype
0.002 0.998 0.000
Q98.7 Male with sex chromosome mosaicism
0.002 0.998 0.000
Q98.6 Male with structurally abnormal sex chromosome
0.002 0.998 0.000
Q98.5 Karyotype 47,XYY
0.002 0.998 0.000
Q98.3 Other male with 46,XX karyotype
0.002 0.998 0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype
0.002 0.998 0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes
0.002 0.998 0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY
0.002 0.998 0.000
D80 Immunodeficiency with predominantly antibody defects
0.002 0.998 0.000
H16 Keratitis
0.002 0.998 0.000
R29 Other symptoms and signs involving the nervous and musculoskeletal systems
0.002 0.998 0.000
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
Q18.0 Sinus, fistula and cyst of branchial cleft
0.002 0.998 0.000
Q07.0 Arnold-Chiari syndrome
0.002 0.998 0.000
Z51.9 Medical care, unspecified
0.000 0.998 0.002
Q85.0 Neurofibromatosis (nonmalignant)
0.002 0.998 0.000
Z98.8 Other specified postsurgical states
0.000 0.998 0.002
G60 Hereditary and idiopathic neuropathy
0.002 0.998 0.000
M10.96 Gout, unspecified (Lower leg)
0.002 0.998 0.000
D23.5 Skin of trunk
0.002 0.998 0.000
H18.8 Other specified disorders of cornea
0.002 0.998 0.000
Z39.0 Care and examination immediately after delivery
0.002 0.998 0.000
H16.0 Corneal ulcer
0.002 0.998 0.000
H66.3 Other chronic suppurative otitis media
0.000 0.998 0.002
K83.9 Disease of biliary tract, unspecified
0.002 0.998 0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver
0.002 0.998 0.000
H16.9 Keratitis, unspecified
0.002 0.998 0.000
H21.9 Disorder of iris and ciliary body, unspecified
0.002 0.998 0.000
H21.4 Pupillary membranes
0.002 0.998 0.000
H21.3 Cyst of iris, ciliary body and anterior chamber
0.002 0.998 0.000
H21.2 Degeneration of iris and ciliary body
0.002 0.998 0.000
H21.1 Other vascular disorders of iris and ciliary body
0.002 0.998 0.000
H74.0 Tympanosclerosis
0.000 0.998 0.002
Q27.3 Peripheral arteriovenous malformation
0.002 0.998 0.000
D80-D89 Certain disorders involving the immune mechanism
0.002 0.998 0.000
H15-H22 Disorders of sclera, cornea, iris and ciliary body
0.002 0.998 0.000
G61.8 Other inflammatory polyneuropathies
0.002 0.998 0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified
0.002 0.998 0.000
Q27.4 Congenital phlebectasia
0.002 0.998 0.000
Q27.2 Other congenital malformations of renal artery
0.002 0.998 0.000
Q27.1 Congenital renal artery stenosis
0.002 0.998 0.000
Q27.0 Congenital absence and hypoplasia of umbilical artery
0.002 0.998 0.000
G64 Other disorders of peripheral nervous system
0.002 0.998 0.000
K85.8 Other acute pancreatitis
0.002 0.998 0.000
K85.3 Drug-induced acute pancreatitis
0.002 0.998 0.000
K85.2 Alcohol-induced acute pancreatitis
0.002 0.998 0.000
K85.0 Idiopathic acute pancreatitis
0.002 0.998 0.000
H65 Nonsuppurative otitis media
0.000 0.998 0.002
K80 Cholelithiasis
0.002 0.998 0.000
E05.8 Other thyrotoxicosis
0.000 0.998 0.002
E05.5 Thyroid crisis or storm
0.000 0.998 0.002
E05.4 Thyrotoxicosis factitia
0.000 0.998 0.002
E05.3 Thyrotoxicosis from ectopic thyroid tissue
0.000 0.998 0.002
E05.1 Thyrotoxicosis with toxic single thyroid nodule
0.000 0.998 0.002
Q38.7 Pharyngeal pouch
0.002 0.998 0.000
H72.8 Other perforations of tympanic membrane
0.000 0.998 0.002
H74.9 Disorder of middle ear and mastoid, unspecified
0.000 0.998 0.002
H74.2 Discontinuity and dislocation of ear ossicles
0.000 0.998 0.002
H74.1 Adhesive middle ear disease
0.000 0.998 0.002
K80.0 Calculus of gallbladder with acute cholecystitis
0.002 0.998 0.000
H74.8 Other specified disorders of middle ear and mastoid
0.000 0.998 0.002
M16.0 Primary coxarthrosis, bilateral
0.002 0.998 0.000
Q90.9 Down's syndrome, unspecified
0.002 0.998 0.000
Q90.2 Trisomy 21, translocation
0.002 0.998 0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q90.0 Trisomy 21, meiotic nondisjunction
0.002 0.998 0.000
Q91.7 Patau's syndrome, unspecified
0.002 0.998 0.000
Q91.6 Trisomy 13, translocation
0.002 0.998 0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q91.4 Trisomy 13, meiotic nondisjunction
0.002 0.998 0.000
Q91.3 Edwards' syndrome, unspecified
0.002 0.998 0.000
Q91.2 Trisomy 18, translocation
0.002 0.998 0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q91.0 Trisomy 18, meiotic nondisjunction
0.002 0.998 0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified
0.002 0.998 0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes
0.002 0.998 0.000
Q92.7 Triploidy and polyploidy
0.002 0.998 0.000
Q92.6 Extra marker chromosomes
0.002 0.998 0.000
Q92.5 Duplications with other complex rearrangements
0.002 0.998 0.000
Q92.4 Duplications seen only at prometaphase
0.002 0.998 0.000
Q92.3 Minor partial trisomy
0.002 0.998 0.000
Q92.2 Major partial trisomy
0.002 0.998 0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction
0.002 0.998 0.000
Q93.9 Deletion from autosomes, unspecified
0.002 0.998 0.000
Q93.8 Other deletions from the autosomes
0.002 0.998 0.000
Q93.7 Deletions with other complex rearrangements
0.002 0.998 0.000
Q93.6 Deletions seen only at prometaphase
0.002 0.998 0.000
Q93.5 Other deletions of part of a chromosome
0.002 0.998 0.000
Q93.4 Deletion of short arm of chromosome 5
0.002 0.998 0.000
Q93.3 Deletion of short arm of chromosome 4
0.002 0.998 0.000
Q93.2 Chromosome replaced with ring or dicentric
0.002 0.998 0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction
0.002 0.998 0.000
Q95.9 Balanced rearrangement and structural marker, unspecified
0.002 0.998 0.000
Q95.8 Other balanced rearrangements and structural markers
0.002 0.998 0.000
Q95.5 Individuals with autosomal fragile site
0.002 0.998 0.000
Q95.4 Individuals with marker heterochromatin
0.002 0.998 0.000

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

The full results table can be downloaded from this page.