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Variant clusters
Hospitalization Episode Statistics (HES)
Genetic variants: 36,212
Diagnostic terms: × 19,155
Association results: = 693,640,860
Self-Reported Statistics (SRS)
Genetic variants: 28,458
Diagnostic terms: × 474
Association results: = 13,489,092
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Variant-specific associations

rs7383287
log Bayes Factor = 68.1186
Chromosome 6   position 32,783,086  (GRCh37) Explore rs7383287 on Ensembl!
Variant rs7383287 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
  
E03.9 Hypothyroidism, unspecified
1.000 0.000 0.000
E05.9 Thyrotoxicosis, unspecified
1.000 0.000 0.000
E05.0 Thyrotoxicosis with diffuse goitre
1.000 0.000 0.000
E10.9 Without complications
1.000 0.000 0.000
E10.3 With ophthalmic complications
1.000 0.000 0.000
E05 Thyrotoxicosis [hyperthyroidism]
1.000 0.000 0.000
E10 Insulin-dependent diabetes mellitus
1.000 0.000 0.000
E10-E14 Diabetes mellitus
1.000 0.000 0.000
E00-E07 Disorders of thyroid gland
1.000 0.000 0.000
H30-H36 Disorders of choroid and retina
1.000 0.000 0.000
Chapter IV Endocrine, nutritional and metabolic diseases
1.000 0.000 0.000
H36.0 Diabetic retinopathy
1.000 0.000 0.000
Chapter VII Diseases of the eye and adnexa
1.000 0.000 0.000
E16.2 Hypoglycaemia, unspecified
1.000 0.000 0.000
E03 Other hypothyroidism
1.000 0.000 0.000
D50-D53 Nutritional anaemias
1.000 0.000 0.000
E16 Other disorders of pancreatic internal secretion
1.000 0.000 0.000
H36 Retinal disorders in diseases classified elsewhere
1.000 0.000 0.000
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion
1.000 0.000 0.000
D50 Iron deficiency anaemia
1.000 0.000 0.000
E10.1 With ketoacidosis
1.000 0.000 0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
1.000 0.000 0.000
E20-E35 Disorders of other endocrine glands
0.999 0.001 0.000
H35 Other retinal disorders
0.999 0.001 0.000
D50.9 Iron deficiency anaemia, unspecified
0.998 0.002 0.000
E27 Other disorders of adrenal gland
0.998 0.002 0.000
E27.1 Primary adrenocortical insufficiency
0.997 0.003 0.000
# Top node
0.997 0.003 0.000
E11 Non-insulin-dependent diabetes mellitus
0.996 0.004 0.000
E11.3 With ophthalmic complications
0.988 0.012 0.000
E10.2 With renal complications
0.984 0.016 0.000
E10.4 With neurological complications
0.984 0.016 0.000
D80-D89 Certain disorders involving the immune mechanism
0.983 0.017 0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.983 0.017 0.000
D50.8 Other iron deficiency anaemias
0.982 0.018 0.000
H00-H06 Disorders of eyelid, lacrimal system and orbit
0.982 0.018 0.000
H06 Disorders of lachrymal system and orbit in diseases classified elsewhere
0.980 0.020 0.000
H06.2 Dysthyroid exophthalmos
0.979 0.021 0.000
D86 Sarcoidosis
0.965 0.035 0.000
E89.0 Postprocedural hypothyroidism
0.961 0.039 0.000
E14 Unspecified diabetes mellitus
0.960 0.040 0.000
E70-E90 Metabolic disorders
0.957 0.043 0.000
E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified
0.956 0.044 0.000
H43-H45 Disorders of vitreous body and globe
0.956 0.044 0.000
H35.2 Other proliferative retinopathy
0.945 0.055 0.000
R31 Unspecified haematuria
0.000 0.062 0.938
D51 Vitamin B12 deficiency anaemia
0.937 0.063 0.000
H35.4 Peripheral retinal degeneration
0.935 0.065 0.000
H43 Disorders of vitreous body
0.932 0.068 0.000
H35.8 Other specified retinal disorders
0.927 0.073 0.000
G50-G59 Nerve, nerve root and plexus disorders
0.924 0.076 0.000
Chapter VI Diseases of the nervous system
0.923 0.077 0.000
D86.9 Sarcoidosis, unspecified
0.922 0.078 0.000
D60-D64 Aplastic and other anaemias
0.918 0.082 0.000
H35.3 Degeneration of macula and posterior pole
0.916 0.084 0.000
Q38-Q45 Other congenital malformations of the digestive system
0.913 0.087 0.000
G51 Facial nerve disorders
0.906 0.094 0.000
H53-H54 Visual disturbances and blindness
0.902 0.098 0.000
E10.0 With coma
0.899 0.101 0.000
H35.0 Background retinopathy and retinal vascular changes
0.895 0.105 0.000
G59 Mononeuropathy in diseases classified elsewhere
0.895 0.105 0.000
Q00-Q07 Congenital malformations of the nervous system
0.893 0.107 0.000
D64 Other anaemias
0.892 0.108 0.000
D51.9 Vitamin B12 deficiency anaemia, unspecified
0.888 0.112 0.000
H10-H13 Disorders of conjunctiva
0.886 0.114 0.000
G56 Mononeuropathies of upper limb
0.884 0.116 0.000
G51.0 Bell's palsy
0.883 0.117 0.000
E14.3 With ophthalmic complications
0.882 0.118 0.000
H53 Visual disturbances
0.878 0.122 0.000
G59.0 Diabetic mononeuropathy
0.874 0.126 0.000
G56.0 Carpal tunnel syndrome
0.874 0.126 0.000
E11.1 With ketoacidosis
0.873 0.127 0.000
H43.8 Other disorders of vitreous body
0.872 0.128 0.000
E11.5 With peripheral circulatory complications
0.865 0.135 0.000
E24 Cushing's syndrome
0.863 0.137 0.000
E11.7 With multiple complications
0.860 0.140 0.000
E10.8 With unspecified complications
0.859 0.141 0.000
H43.1 Vitreous haemorrhage
0.858 0.142 0.000
E28 Ovarian dysfunction
0.855 0.145 0.000
D64.9 Anaemia, unspecified
0.854 0.146 0.000
E40-E46 Malnutrition
0.854 0.146 0.000
H49-H52 Disorders of ocular muscles, binocular movement, accommodation and refraction
0.853 0.147 0.000
E16.0 Drug-induced hypoglycaemia without coma
0.850 0.150 0.000
G00-G09 Inflammatory diseases of the central nervous system
0.846 0.154 0.000
D86.8 Sarcoidosis of other and combined sites
0.839 0.161 0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver
0.839 0.161 0.000
E78 Disorders of lipoprotein metabolism and other lipidaemias
0.838 0.162 0.000
E16.1 Other hypoglycaemia
0.836 0.164 0.000
E14.8 With unspecified complications
0.830 0.170 0.000
H15-H22 Disorders of sclera, cornea, iris and ciliary body
0.830 0.170 0.000
H50 Other strabismus
0.827 0.173 0.000
H33 Retinal detachments and breaks
0.823 0.177 0.000
E10.7 With multiple complications
0.821 0.179 0.000
D50.1 Sideropenic dysphagia
0.821 0.179 0.000
H53.1 Subjective visual disturbances
0.818 0.182 0.000
E03.2 Hypothyroidism due to medicaments and other exogenous substances
0.815 0.185 0.000
D53 Other nutritional anaemias
0.811 0.189 0.000
Q50-Q56 Congenital malformations of genital organs
0.808 0.192 0.000
H05 Disorders of orbit
0.806 0.194 0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
0.805 0.195 0.000
D52 Folate deficiency anaemia
0.804 0.196 0.000
Q20-Q28 Congenital malformations of the circulatory system
0.801 0.199 0.000
E06 Thyroiditis
0.798 0.202 0.000
E78.9 Disorder of lipoprotein metabolism, unspecified
0.795 0.205 0.000
Q05 Spina bifida
0.795 0.205 0.000
H53.9 Visual disturbance, unspecified
0.793 0.207 0.000
E10.5 With peripheral circulatory complications
0.791 0.209 0.000
H46-H48 Disorders of optic nerve and visual pathways
0.786 0.214 0.000
H30 Chorioretinal inflammation
0.785 0.215 0.000
E20 Hypoparathyroidism
0.782 0.218 0.000
E65-E68 Obesity and other hyperalimentation
0.780 0.220 0.000
H11 Other disorders of conjunctiva
0.778 0.222 0.000
E85 Amyloidosis
0.777 0.223 0.000
Q35-Q37 Cleft lip and cleft palate
0.776 0.224 0.000
G08 Intracranial and intraspinal phlebitis and thrombophlebitis
0.774 0.226 0.000
D86.3 Sarcoidosis of skin
0.774 0.226 0.000
H33.1 Retinoschisis and retinal cysts
0.773 0.227 0.000
E50-E64 Other nutritional deficiencies
0.772 0.228 0.000
D64.8 Other specified anaemias
0.770 0.230 0.000
E31 Polyglandular dysfunction
0.769 0.231 0.000
H50.0 Convergent concomitant strabismus
0.769 0.231 0.000
E11.0 With coma
0.766 0.234 0.000
M35.0 Sicca syndrome [Sjogren]
0.762 0.238 0.000
H35.6 Retinal haemorrhage
0.762 0.238 0.000
E10.6 With other specified complications
0.761 0.239 0.000
H53.0 Amblyopia ex anopsia
0.761 0.239 0.000
E14.2 Withrenal complications
0.761 0.239 0.000
E21 Hyperparathyroidism and other disorders of parathyroid gland
0.760 0.240 0.000
H53.2 Diplopia
0.760 0.240 0.000
E11.4 With neurological complications
0.758 0.242 0.000
Q38 Other congenital malformations of tongue, mouth and pharynx
0.757 0.243 0.000
Q44.6 Cystic disease of liver
0.754 0.246 0.000
M35 Other systemic involvement of connective tissue
0.754 0.246 0.000
E46 Unspecified protein-energy malnutrition
0.749 0.251 0.000
E70 Disorders of aromatic amino-acid metabolism
0.747 0.253 0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.744 0.255 0.000
M20-M25 Other joint disorders
0.743 0.257 0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.742 0.258 0.000
D82 Immunodeficiency associated with other major defects
0.741 0.259 0.000
Chapter XIII Diseases of the musculoskeletal system and connective tissue
0.741 0.259 0.000
D80 Immunodeficiency with predominantly antibody defects
0.740 0.260 0.000
E03.8 Other specified hypothyroidism
0.740 0.260 0.000
E14.5 With peripheral circulatory complications
0.739 0.261 0.000
D83 Common variable immunodeficiency
0.739 0.261 0.000
E11.6 With other specified complications
0.738 0.262 0.000
G52 Disorders of other cranial nerves
0.736 0.264 0.000
H18 Other disorders of cornea
0.735 0.265 0.000
G51.9 Disorder of facial nerve, unspecified
0.734 0.265 0.000
E28.3 Primary ovarian failure
0.733 0.267 0.000
E78.8 Other disorders of lipoprotein metabolism
0.733 0.267 0.000
H33.4 Traction detachment of retina
0.730 0.270 0.000
H01 Other inflammation of eyelid
0.729 0.271 0.000
E14.1 With ketoacidosis
0.728 0.272 0.000
Q05.9 Spina bifida, unspecified
0.725 0.275 0.000
E27.3 Drug-induced adrenocortical insufficiency
0.718 0.282 0.000
H43.9 Disorder of vitreous body, unspecified
0.718 0.282 0.000
D55-D59 Haemolytic anaemias
0.717 0.283 0.000
E05.5 Thyroid crisis or storm
0.717 0.283 0.000
E05.4 Thyrotoxicosis factitia
0.717 0.283 0.000
E05.3 Thyrotoxicosis from ectopic thyroid tissue
0.717 0.283 0.000
E05.1 Thyrotoxicosis with toxic single thyroid nodule
0.717 0.283 0.000
E01 Iodine-deficiency-related thyroid disorders and allied conditions
0.717 0.283 0.000
E00 Congenital iodine-deficiency syndrome
0.717 0.283 0.000
E12 Malnutrition-related diabetes mellitus
0.717 0.283 0.000
H32 Chorioretinal disorders in diseases classified elsewhere
0.717 0.283 0.000
E03.5 Myxoedema coma
0.717 0.283 0.000
E03.4 Atrophy of thyroid (acquired)
0.717 0.283 0.000
E03.3 Postinfectious hypothyroidism
0.717 0.283 0.000
E03.1 Congenital hypothyroidism without goitre
0.717 0.283 0.000
E03.0 Congenital hypothyroidism with diffuse goitre
0.717 0.283 0.000
E16.9 Disorder of pancreatic internal secretion, unspecified
0.717 0.283 0.000
E16.8 Other specified disorders of pancreatic internal secretion
0.717 0.283 0.000
E16.4 Abnormal secretion of gastrin
0.717 0.283 0.000
E16.3 Increased secretion of glucagon
0.717 0.283 0.000
H36.8 Other retinal disorders in diseases classified elsewhere
0.717 0.283 0.000
E15 Nondiabetic hypoglycaemic coma
0.717 0.283 0.000
H43.2 Crystalline deposits in vitreous body
0.717 0.283 0.000
E29 Testicular dysfunction
0.717 0.283 0.000
E35 Disorders of endocrine glands in diseases classified elsewhere
0.716 0.284 0.000
E32 Diseases of thymus
0.716 0.284 0.000
E30 Disorders of puberty, not elsewhere classified
0.716 0.284 0.000
E25 Adrenogenital disorders
0.716 0.284 0.000
H35.1 Retinopathy of prematurity
0.716 0.284 0.000
E27.5 Adrenomedullary hyperfunction
0.715 0.285 0.000
E27.0 Other adrenocortical overactivity
0.715 0.285 0.000
Chapter XVI Certain conditions originating in the perinatal period
0.715 0.285 0.000
E79 Disorders of purine and pyrimidine metabolism
0.714 0.286 0.000
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.714 0.286 0.000
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)
0.712 0.288 0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.711 0.289 0.000
E89.4 Postprocedural ovarian failure
0.710 0.289 0.000
M21 Other acquired deformities of limbs
0.710 0.290 0.000
H15 Disorders of sclera
0.708 0.292 0.000
D86.1 Sarcoidosis of lymph nodes
0.706 0.294 0.000
H35.5 Hereditary retinal dystrophy
0.706 0.294 0.000
G56.9 Mononeuropathy of upper limb, unspecified
0.705 0.295 0.000
D81 Combined immunodeficiencies
0.705 0.295 0.000
Q30-Q34 Congenital malformations of the respiratory system
0.704 0.295 0.000
H06.3 Other disorders of orbit in diseases classified elsewhere
0.703 0.297 0.000
H06.1 Parasitic infestation of orbit in diseases classified elsewhere
0.703 0.297 0.000
H06.0 Disorders of lachrymal system in diseases classified elsewhere
0.703 0.297 0.000
E24.2 Drug-induced Cushing's syndrome
0.702 0.298 0.000
D65 Disseminated intravascular coagulation [defibrination syndrome]
0.701 0.299 0.000
G10-G14 Systemic atrophies primarily affecting the central nervous system
0.701 0.299 0.000
G56.4 Causalgia
0.700 0.300 0.000
H19 Disorders of sclera and cornea in diseases classified elsewhere
0.696 0.304 0.000
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
0.696 0.304 0.000
H10 Conjunctivitis
0.696 0.304 0.000
E27.8 Other specified disorders of adrenal gland
0.695 0.305 0.000
G51.8 Other disorders of facial nerve
0.695 0.305 0.000
Q22 Congenital malformations of pulmonary and tricuspid valves
0.694 0.306 0.000
G00 Bacterial meningitis, not elsewhere classified
0.694 0.306 0.000
G53 Cranial nerve disorders in diseases classified elsewhere
0.693 0.307 0.000
Q44.5 Other congenital malformations of bile ducts
0.692 0.308 0.000
H18.4 Corneal degeneration
0.692 0.308 0.000
E14.7 With multiple complications
0.688 0.312 0.000
E14.0 With coma
0.688 0.312 0.000
E24.8 Other Cushing's syndrome
0.688 0.312 0.000
E05.8 Other thyrotoxicosis
0.686 0.313 0.000
E77 Disorders of glycoprotein metabolism
0.686 0.314 0.000
E76 Disorders of glycosaminoglycan metabolism
0.686 0.314 0.000
E75 Disorders of sphingolipid metabolism and other lipid storage disorders
0.686 0.314 0.000
E72 Other disorders of amino-acid metabolism
0.686 0.314 0.000
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
0.686 0.314 0.000
E90 Nutritional and metabolic disorders in diseases classified elsewhere
0.686 0.314 0.000
H11.0 Pterygium
0.686 0.314 0.000
E89.9 Postprocedural endocrine and metabolic disorder, unspecified
0.686 0.314 0.000
E89.8 Other postprocedural endocrine and metabolic disorders
0.686 0.314 0.000
E89.5 Postprocedural testicular hypofunction
0.686 0.314 0.000
E89.1 Postprocedural hypoinsulinaemia
0.686 0.314 0.000
H45 Disorders of vitreous body and globe in diseases classified elsewhere
0.685 0.315 0.000
M34 Systemic sclerosis
0.685 0.315 0.000
E73 Lactose intolerance
0.685 0.315 0.000
Q04 Other congenital malformations of brain
0.683 0.317 0.000
Q43 Other congenital malformations of intestine
0.683 0.317 0.000
D84 Other immunodeficiencies
0.681 0.319 0.000
H50.8 Other specified strabismus
0.681 0.319 0.000
E78.6 Lipoprotein deficiency
0.680 0.320 0.000
H05.2 Exophthalmic conditions
0.678 0.322 0.000
D53.9 Nutritional anaemia, unspecified
0.676 0.324 0.000
H50.4 Other and unspecified heterotropia
0.676 0.324 0.000
E02 Subclinical iodine-deficiency hypothyroidism
0.675 0.325 0.000
G58 Other mononeuropathies
0.674 0.326 0.000
Q07 Other congenital malformations of nervous system
0.674 0.326 0.000
E27.4 Other and unspecified adrenocortical insufficiency
0.673 0.327 0.000
D51.8 Other vitamin B12 deficiency anaemias
0.672 0.328 0.000
D51.3 Other dietary vitamin B12 deficiency anaemia
0.672 0.328 0.000
D51.2 Transcobalamin II deficiency
0.672 0.328 0.000
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria
0.672 0.328 0.000
G54 Nerve root and plexus disorders
0.671 0.328 0.000
E78.4 Other hyperlipidaemia
0.671 0.329 0.000
H43.0 Vitreous prolapse
0.668 0.331 0.000
Q60-Q64 Congenital malformations of the urinary system
0.667 0.333 0.000
Q27 Other congenital malformations of peripheral vascular system
0.666 0.334 0.000
D52.9 Folate deficiency anaemia, unspecified
0.663 0.337 0.000
G09 Sequelae of inflammatory diseases of central nervous system
0.663 0.337 0.000
E84 Cystic fibrosis
0.662 0.338 0.000
Q03 Congenital hydrocephalus
0.661 0.339 0.000
G56.1 Other lesions of median nerve
0.661 0.339 0.000
E27.9 Disorder of adrenal gland, unspecified
0.660 0.340 0.000
H50.5 Heterophoria
0.659 0.341 0.000
D86.0 Sarcoidosis of lung
0.658 0.342 0.000
D60 Acquired pure red cell aplasia [erythroblastopenia]
0.658 0.342 0.000
E22 Hyperfunction of pituitary gland
0.657 0.343 0.000
E24.0 Pituitary-dependent Cushing's disease
0.656 0.344 0.000
E23 Hypofunction and other disorders of pituitary gland
0.656 0.344 0.000
E78.2 Mixed hyperlipidaemia
0.655 0.345 0.000
Q45 Other congenital malformations of digestive system
0.654 0.345 0.000
Q42 Congenital absence, atresia and stenosis of large intestine
0.654 0.345 0.000
Q41 Congenital absence, atresia and stenosis of small intestine
0.654 0.345 0.000
E13 Other specified diabetes mellitus
0.654 0.346 0.000
E14.4 With neurological complications
0.654 0.346 0.000
M21.0 Valgus deformity, not elsewhere classified
0.654 0.346 0.000
Q55 Other congenital malformations of male genital organs
0.653 0.347 0.000
E06.3 Autoimmune thyroiditis
0.651 0.349 0.000
E28.2 Polycystic ovarian syndrome
0.651 0.349 0.000
Q80-Q89 Other congenital malformations
0.651 0.349 0.000
G51.4 Facial myokymia
0.649 0.351 0.000
G51.2 Melkersson's syndrome
0.649 0.351 0.000
G51.1 Geniculate ganglionitis
0.649 0.351 0.000
G30-G32 Other degenerative diseases of the nervous system
0.649 0.351 0.000
H31 Other disorders of choroid
0.648 0.352 0.000
E11.8 With unspecified complications
0.648 0.352 0.000
E14.9 Without complications
0.646 0.354 0.000
Q50 Congenital malformations of ovaries, Fallopian tubes and broad ligaments
0.645 0.355 0.000
E85.4 Organ-limited amyloidosis
0.645 0.355 0.000
H11.9 Disorder of conjunctiva, unspecified
0.644 0.356 0.000
E14.6 With other specified complications
0.642 0.358 0.000
G59.8 Other mononeuropathies in diseases classified elsewhere
0.642 0.358 0.000
Q06 Other congenital malformations of spinal cord
0.640 0.360 0.000
Q01 Encephalocele
0.640 0.360 0.000
Q00 Anencephaly and similar malformations
0.640 0.360 0.000
Q02 Microcephaly
0.640 0.360 0.000
M15-M19 Arthrosis
0.640 0.360 0.000
D64.4 Congenital dyserythropoietic anaemia
0.639 0.360 0.000
D64.3 Other sideroblastic anaemias
0.639 0.360 0.000
D64.2 Secondary sideroblastic anaemia due to drugs and toxins
0.639 0.360 0.000
D64.1 Secondary sideroblastic anaemia due to disease
0.639 0.360 0.000
D64.0 Hereditary sideroblastic anaemia
0.639 0.360 0.000
D89.9 Disorder involving the immune mechanism, unspecified
0.638 0.362 0.000
G04 Encephalitis, myelitis and encephalomyelitis
0.638 0.362 0.000
M18 Arthrosis of first carpometacarpal joint
0.638 0.362 0.000
G50 Disorders of trigeminal nerve
0.637 0.363 0.000
M32 Systemic lupus erythematosus
0.636 0.364 0.000
H13 Disorders of conjunctiva in diseases classified elsewhere
0.635 0.365 0.000
H02 Other disorders of eyelid
0.634 0.366 0.000
E66 Obesity
0.634 0.366 0.000
Q38.7 Pharyngeal pouch
0.634 0.366 0.000
E53 Deficiency of other B group vitamins
0.633 0.367 0.000
Q28 Other congenital malformations of circulatory system
0.633 0.367 0.000
D69 Purpura and other haemorrhagic conditions
0.633 0.367 0.000
E27.2 Addisonian crisis
0.633 0.367 0.000
H30.9 Chorioretinal inflammation, unspecified
0.631 0.369 0.000
H16 Keratitis
0.631 0.369 0.000
H50.9 Strabismus, unspecified
0.631 0.369 0.000
G51.3 Clonic hemifacial spasm
0.630 0.370 0.000
G05 Encephalitis, myelitis and encephalomyelitis in diseases classified elsewhere
0.630 0.370 0.000
H53.6 Night blindness
0.630 0.370 0.000
H53.5 Colour vision deficiencies
0.630 0.370 0.000
H53.3 Other disorders of binocular vision
0.630 0.370 0.000
E80 Disorders of porphyrin and bilirubin metabolism
0.629 0.371 0.000
M86-M90 Other osteopathies
0.628 0.372 0.000
E89.6 Postprocedural adrenocortical(-medullary) hypofunction
0.627 0.373 0.000
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.627 0.373 0.000
H34 Retinal vascular occlusions
0.627 0.373 0.000
H03 Disorders of eyelid in diseases classified elsewhere
0.626 0.373 0.000
E20.9 Hypoparathyroidism, unspecified
0.626 0.374 0.000
Q40 Other congenital malformations of upper alimentary tract
0.626 0.374 0.000
H01.9 Inflammation of eyelid, unspecified
0.625 0.375 0.000
G02 Meningitis in other infectious and parasitic diseases classified elsewhere
0.624 0.376 0.000
G52.9 Cranial nerve disorder, unspecified
0.623 0.377 0.000
H11.8 Other specified disorders of conjunctiva
0.623 0.377 0.000
M18.0 Primary arthrosis of first carpometacarpal joints, bilateral
0.622 0.378 0.000
R30-R39 Symptoms and signs involving the urinary system
0.000 0.378 0.622
H15.8 Other disorders of sclera
0.621 0.379 0.000
Q51 Congenital malformations of uterus and cervix
0.620 0.380 0.000
E56 Other vitamin deficiencies
0.620 0.380 0.000
E24.9 Cushing's syndrome, unspecified
0.620 0.380 0.000
E21.1 Secondary hyperparathyroidism, not elsewhere classified
0.619 0.381 0.000
E24.4 Alcohol-induced pseudo-Cushing's syndrome
0.619 0.381 0.000
E24.3 Ectopic ACTH syndrome
0.619 0.381 0.000
E24.1 Nelson's syndrome
0.619 0.381 0.000
Q39 Congenital malformations of oesophagus
0.618 0.382 0.000
M21.06 Valgus deformity, not elsewhere classified (Lower leg)
0.618 0.382 0.000
H35.7 Separation of retinal layers
0.617 0.383 0.000
H18.3 Changes in corneal membranes
0.616 0.384 0.000
E07 Other disorders of thyroid
0.615 0.385 0.000
M35.7 Hypermobility syndrome
0.614 0.386 0.000
G70-G73 Diseases of myoneural junction and muscle
0.613 0.386 0.000
E11.2 With renal complications
0.613 0.387 0.000
E28.9 Ovarian dysfunction, unspecified
0.613 0.387 0.000
E28.8 Other ovarian dysfunction
0.613 0.387 0.000
E28.1 Androgen excess
0.613 0.387 0.000
E28.0 Oestrogen excess
0.613 0.387 0.000
E44 Protein-energy malnutrition of moderate and mild degree
0.612 0.388 0.000
E45 Retarded development following protein-energy malnutrition
0.612 0.388 0.000
E43 Unspecified severe protein-energy malnutrition
0.612 0.388 0.000
E42 Marasmic kwashiorkor
0.612 0.388 0.000
E41 Nutritional marasmus
0.612 0.388 0.000
E40 Kwashiorkor
0.612 0.388 0.000
M22 Disorders of patella
0.611 0.389 0.000
Q22.1 Congenital pulmonary valve stenosis
0.609 0.391 0.000
H01.8 Other specified inflammation of eyelid
0.607 0.392 0.000
M21.3 Wrist or foot drop (acquired)
0.607 0.393 0.000
G07 Intracranial and intraspinal abscess and granuloma in diseases classified elsewhere
0.606 0.394 0.000
H18.8 Other specified disorders of cornea
0.605 0.395 0.000
E31.0 Autoimmune polyglandular failure
0.604 0.395 0.000
E85.9 Amyloidosis, unspecified
0.604 0.396 0.000
Q44.7 Other congenital malformations of liver
0.602 0.398 0.000
Q44.4 Choledochal cyst
0.602 0.398 0.000
Q44.3 Congenital stenosis and stricture of bile ducts
0.602 0.398 0.000
Q44.2 Atresia of bile ducts
0.602 0.398 0.000
Q44.1 Other congenital malformations of gallbladder
0.602 0.398 0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder
0.602 0.398 0.000
H46 Optic neuritis
0.601 0.399 0.000
H10.9 Conjunctivitis, unspecified
0.601 0.399 0.000
E78.3 Hyperchylomicronaemia
0.601 0.399 0.000
H47 Other disorders of optic [2nd] nerve and visual pathways
0.600 0.400 0.000
D63 Anaemia in chronic diseases classified elsewhere
0.600 0.400 0.000
Q35 Cleft palate
0.599 0.401 0.000
R35 Polyuria
0.000 0.402 0.598
E21.2 Other hyperparathyroidism
0.598 0.402 0.000
H05.0 Acute inflammation of orbit
0.598 0.402 0.000
E06.5 Other chronic thyroiditis
0.598 0.402 0.000
M35.1 Other overlap syndromes
0.596 0.403 0.000
E70.3 Albinism
0.596 0.404 0.000
E66.8 Other obesity
0.596 0.404 0.000
D61 Other aplastic anaemias
0.595 0.405 0.000
R30 Pain associated with micturition
0.000 0.406 0.594
H50.6 Mechanical strabismus
0.593 0.407 0.000
H50.3 Intermittent heterotropia
0.593 0.407 0.000
E74 Other disorders of carbohydrate metabolism
0.592 0.407 0.000
M60-M63 Disorders of muscles
0.593 0.407 0.000
G03 Meningitis due to other and unspecified causes
0.592 0.407 0.000
Q37 Cleft palate with cleft lip
0.592 0.408 0.000
H51 Other disorders of binocular movement
0.591 0.409 0.000
M18.1 Other primary arthrosis of first carpometacarpal joint
0.591 0.409 0.000
H44 Disorders of globe
0.591 0.409 0.000
H50.2 Vertical strabismus
0.587 0.413 0.000
M22.2 Patellofemoral disorders
0.586 0.414 0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.585 0.415 0.000
R30.0 Dysuria
0.000 0.417 0.583
Q52 Other congenital malformations of female genitalia
0.582 0.418 0.000
D53.8 Other specified nutritional anaemias
0.582 0.418 0.000
D53.2 Scorbutic anaemia
0.582 0.418 0.000
D53.1 Other megaloblastic anaemias, not elsewhere classified
0.582 0.418 0.000
D53.0 Protein deficiency anaemia
0.582 0.418 0.000
E51 Thiamine deficiency
0.581 0.419 0.000
M21.7 Unequal limb length (acquired)
0.581 0.419 0.000
E78.1 Pure hyperglyceridaemia
0.581 0.419 0.000
M00-M03 Infectious arthropathies
0.580 0.420 0.000
Q56 Indeterminate sex and pseudohermaphroditism
0.579 0.421 0.000
H05.9 Disorder of orbit, unspecified
0.578 0.422 0.000
H05.5 Retained (old) foreign body following penetrating wound of orbit
0.578 0.422 0.000
H05.4 Enophthalmos
0.578 0.422 0.000
H05.3 Deformity of orbit
0.578 0.422 0.000
H05.1 Chronic inflammatory disorders of orbit
0.578 0.422 0.000
D67 Hereditary factor IX deficiency
0.577 0.422 0.000
D52.8 Other folate deficiency anaemias
0.576 0.424 0.000
D52.1 Drug-induced folate deficiency anaemia
0.576 0.424 0.000
D52.0 Dietary folate deficiency anaemia
0.576 0.424 0.000
H22 Disorders of iris and ciliary body in diseases classified elsewhere
0.575 0.425 0.000
Q26 Congenital malformations of great veins
0.574 0.426 0.000
Q20 Congenital malformations of cardiac chambers and connexions
0.574 0.426 0.000
Q43.3 Congenital malformations of intestinal fixation
0.572 0.428 0.000
E06.4 Drug-induced thyroiditis
0.572 0.428 0.000
E06.2 Chronic thyroiditis with transient thyrotoxicosis
0.572 0.428 0.000
E06.1 Subacute thyroiditis
0.572 0.428 0.000
E06.0 Acute thyroiditis
0.572 0.428 0.000
M34.0 Progressive systemic sclerosis
0.571 0.429 0.000
E26 Hyperaldosteronism
0.571 0.429 0.000
D89.1 Cryoglobulinaemia
0.571 0.429 0.000
H18.1 Bullous keratopathy
0.570 0.430 0.000
Q05.8 Sacral spina bifida without hydrocephalus
0.570 0.430 0.000
Q05.7 Lumbar spina bifida without hydrocephalus
0.570 0.430 0.000
Q05.6 Thoracic spina bifida without hydrocephalus
0.570 0.430 0.000
Q05.5 Cervical spina bifida without hydrocephalus
0.570 0.430 0.000
Q05.4 Unspecified spina bifida with hydrocephalus
0.570 0.430 0.000
Q05.3 Sacral spina bifida with hydrocephalus
0.570 0.430 0.000
Q05.2 Lumbar spina bifida with hydrocephalus
0.570 0.430 0.000
Q05.1 Thoracic spina bifida with hydrocephalus
0.570 0.430 0.000
Q05.0 Cervical spina bifida with hydrocephalus
0.570 0.430 0.000
H19.3 Keratitis and keratoconjunctivitis in other diseases classified elsewhere
0.568 0.432 0.000
M34.9 Systemic sclerosis, unspecified
0.568 0.432 0.000
D82.1 Di George's syndrome
0.567 0.433 0.000
Q23 Congenital malformations of aortic and mitral valves
0.566 0.434 0.000
Q53 Undescended testicle
0.566 0.434 0.000
G11 Hereditary ataxia
0.565 0.434 0.000
Q38.6 Other congenital malformations of mouth
0.563 0.437 0.000
H48 Disorders of optic [2nd] nerve and visual pathways in diseases classified elsewhere
0.563 0.437 0.000
D83.9 Common variable immunodeficiency, unspecified
0.563 0.437 0.000
H30.8 Other chorioretinal inflammations
0.563 0.437 0.000
H30.2 Posterior cyclitis
0.563 0.437 0.000
H30.1 Disseminated chorioretinal inflammation
0.563 0.437 0.000
H30.0 Focal chorioretinal inflammation
0.563 0.437 0.000
H05.8 Other disorders of orbit
0.561 0.439 0.000
E20.8 Other hypoparathyroidism
0.560 0.439 0.000
E20.1 Pseudohypoparathyroidism
0.560 0.439 0.000
E20.0 Idiopathic hypoparathyroidism
0.560 0.439 0.000
M32.1 Systemic lupus erythematosus with organ or system involvement
0.560 0.440 0.000
E88 Other metabolic disorders
0.560 0.440 0.000
G00.1 Pneumococcal meningitis
0.560 0.440 0.000
Q99 Other chromosome abnormalities, not elsewhere classified
0.559 0.441 0.000
E67 Other hyperalimentation
0.559 0.441 0.000
E68 Sequelae of hyperalimentation
0.559 0.441 0.000
E53.8 Deficiency of other specified B group vitamins
0.557 0.443 0.000
E85.8 Other amyloidosis
0.557 0.443 0.000
E85.2 Heredofamilial amyloidosis, unspecified
0.557 0.443 0.000
E85.1 Neuropathic heredofamilial amyloidosis
0.557 0.443 0.000
E85.0 Nonneuropathic heredofamilial amyloidosis
0.557 0.443 0.000
G04.8 Other encephalitis, myelitis and encephalomyelitis
0.556 0.444 0.000
Q36 Cleft lip
0.556 0.444 0.000
D68 Other coagulation defects
0.556 0.444 0.000
G58.9 Mononeuropathy, unspecified
0.556 0.444 0.000
M34.1 CR(E)ST syndrome
0.555 0.445 0.000
E64 Sequelae of malnutrition and other nutritional deficiencies
0.554 0.446 0.000
E63 Other nutritional deficiencies
0.554 0.446 0.000
E50 Vitamin A deficiency
0.554 0.446 0.000
E60 Dietary zinc deficiency
0.554 0.446 0.000
E59 Dietary selenium deficiency
0.554 0.446 0.000
E58 Dietary calcium deficiency
0.554 0.446 0.000
E54 Ascorbic acid deficiency
0.554 0.446 0.000
E52 Niacin deficiency [pellagra]
0.554 0.446 0.000
E31.9 Polyglandular dysfunction, unspecified
0.551 0.448 0.000
E31.8 Other polyglandular dysfunction
0.551 0.448 0.000
E31.1 Polyglandular hyperfunction
0.551 0.448 0.000
Q18 Other congenital malformations of face and neck
0.551 0.449 0.000
H11.1 Conjunctival degenerations and deposits
0.551 0.449 0.000
M35.3 Polymyalgia rheumatica
0.551 0.449 0.000
Q43.9 Congenital malformation of intestine, unspecified
0.551 0.449 0.000
M21.2 Flexion deformity
0.550 0.450 0.000
H19.1 Herpesviral keratitis and keratoconjunctivitis
0.550 0.450 0.000
H53.4 Visual field defects
0.549 0.451 0.000
H33.3 Retinal breaks without detachment
0.548 0.452 0.000
Q27.9 Congenital malformation of peripheral vascular system, unspecified
0.548 0.452 0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
0.548 0.452 0.000
D69.4 Other primary thrombocytopenia
0.548 0.452 0.000
E06.9 Thyroiditis, unspecified
0.546 0.454 0.000
M88 Paget's disease of bone [osteitis deformans]
0.545 0.455 0.000
E21.5 Disorder of parathyroid gland, unspecified
0.545 0.455 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.

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