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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

rs805285
log Bayes Factor = 12.3599
Chromosome 6   position 31,679,465  (GRCh37) Explore rs805285 on Ensembl!

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
  
K90.0 Coeliac disease
0.000 0.000 1.000
E10 Insulin-dependent diabetes mellitus
0.986 0.014 0.000
E10.9 Without complications
0.974 0.026 0.000
E10.4 With neurological complications
0.974 0.026 0.000
E10.3 With ophthalmic complications
0.969 0.031 0.000
E10.5 With peripheral circulatory complications
0.896 0.104 0.000
E10.0 With coma
0.864 0.136 0.000
K50 Crohn's disease [regional enteritis]
0.840 0.160 0.000
K50.1 Crohn's disease of large intestine
0.838 0.162 0.000
E10.2 With renal complications
0.834 0.166 0.000
K50.0 Crohn's disease of small intestine
0.824 0.176 0.000
K50.9 Crohn's disease, unspecified
0.803 0.197 0.000
E10.1 With ketoacidosis
0.797 0.203 0.000
E10-E14 Diabetes mellitus
0.754 0.245 0.001
J45.9 Asthma, unspecified
0.000 0.255 0.745
K50.8 Other Crohn's disease
0.732 0.268 0.000
E10.6 With other specified complications
0.707 0.293 0.000
E10.7 With multiple complications
0.707 0.293 0.000
E13 Other specified diabetes mellitus
0.705 0.294 0.001
E13.9 Without complications
0.671 0.329 0.000
E11 Non-insulin-dependent diabetes mellitus
0.605 0.395 0.000
E11.4 With neurological complications
0.576 0.424 0.000
E10.8 With unspecified complications
0.569 0.430 0.000
L43.9 Lichen planus, unspecified
0.564 0.436 0.000
E11.0 With coma
0.559 0.441 0.000
K50-K52 Noninfective enteritis and colitis
0.554 0.446 0.000
L43 Lichen planus
0.551 0.449 0.000
L40 Psoriasis
0.548 0.452 0.000
L40.5 Arthropathic psoriasis
0.547 0.453 0.000
L40-L45 Papulosquamous disorders
0.543 0.457 0.000
E12 Malnutrition-related diabetes mellitus
0.540 0.459 0.001
E11.6 With other specified complications
0.527 0.473 0.000
E13.8 With unspecified complications
0.506 0.494 0.001
E13.7 With multiple complications
0.506 0.494 0.001
E13.6 With other specified complications
0.506 0.494 0.001
E13.5 With peripheral circulatory complications
0.506 0.494 0.001
E13.4 With neurological complications
0.506 0.494 0.001
E13.3 With ophthalmic complications
0.506 0.494 0.001
E13.2 With renal complications
0.506 0.494 0.001
E13.1 With ketoacidosis
0.506 0.494 0.001
E13.0 With coma
0.506 0.494 0.001
K52 Other non-infective gastro-enteritis and colitis
0.498 0.502 0.000
E11.5 With peripheral circulatory complications
0.478 0.522 0.000
K52.8 Other specified non-infective gastro-enteritis and colitis
0.467 0.533 0.000
L40.9 Psoriasis, unspecified
0.457 0.543 0.000
L40.4 Guttate psoriasis
0.456 0.544 0.000
E11.7 With multiple complications
0.434 0.566 0.000
L40.1 Generalised pustular psoriasis
0.432 0.568 0.000
J45 Asthma
0.000 0.575 0.425
E14 Unspecified diabetes mellitus
0.423 0.577 0.000
K52.0 Gastro-enteritis and colitis due to radiation
0.422 0.578 0.000
K52.3 Indeterminate colitis
0.415 0.585 0.000
L42 Pityriasis rosea
0.398 0.602 0.000
L40.8 Other psoriasis
0.397 0.602 0.000
L43.3 Subacute (active) lichen planus
0.395 0.605 0.000
L43.2 Lichenoid drug reaction
0.395 0.605 0.000
L43.1 Bullous lichen planus
0.395 0.605 0.000
L43.0 Hypertrophic lichen planus
0.395 0.605 0.000
L40.3 Pustulosis palmaris et plantaris
0.393 0.607 0.000
L40.2 Acrodermatitis continua
0.393 0.607 0.000
K51 Ulcerative colitis
0.393 0.607 0.000
K52.1 Toxic gastro-enteritis and colitis
0.392 0.608 0.000
L44 Other papulosquamous disorders
0.389 0.610 0.000
L41 Parapsoriasis
0.389 0.610 0.000
L45 Papulosquamous disorders in diseases classified elsewhere
0.389 0.610 0.000
E12.9 Without complications
0.387 0.612 0.001
E12.8 With unspecified complications
0.387 0.612 0.001
E12.7 With multiple complications
0.387 0.612 0.001
E12.6 With other specified complications
0.387 0.612 0.001
E12.5 With peripheral circulatory complications
0.387 0.612 0.001
E12.4 With neurological complications
0.387 0.612 0.001
E12.3 With ophthalmic complications
0.387 0.612 0.001
E12.2 With renal complications
0.387 0.612 0.001
E12.1 With ketoacidosis
0.387 0.612 0.001
E12.0 With coma
0.387 0.612 0.001
L43.8 Other lichen planus
0.383 0.617 0.000
J45.0 Predominantly allergic asthma
0.000 0.626 0.374
E11.2 With renal complications
0.360 0.640 0.000
E11.1 With ketoacidosis
0.355 0.645 0.000
L40.0 Psoriasis vulgaris
0.348 0.652 0.000
E14.6 With other specified complications
0.339 0.661 0.000
K51.3 Ulcerative (chronic) rectosigmoiditis
0.334 0.666 0.000
E14.8 With unspecified complications
0.327 0.672 0.000
E14.4 With neurological complications
0.325 0.675 0.000
E14.5 With peripheral circulatory complications
0.321 0.679 0.000
E11.8 With unspecified complications
0.320 0.680 0.000
K51.4 Pseudopolyposis of colon
0.310 0.690 0.000
E14.1 With ketoacidosis
0.306 0.694 0.000
E14.7 With multiple complications
0.303 0.697 0.000
E14.0 With coma
0.303 0.697 0.000
J45.1 Nonallergic asthma
0.000 0.697 0.303
K51.2 Ulcerative (chronic) proctitis
0.298 0.702 0.000
E14.2 Withrenal complications
0.298 0.702 0.000
K90 Intestinal malabsorption
0.000 0.704 0.296
K51.5 Mucosal proctocolitis
0.288 0.712 0.000
K52.2 Allergic and dietetic gastro-enteritis and colitis
0.286 0.714 0.000
D69.6 Thrombocytopenia, unspecified
0.000 0.717 0.283
L41.9 Parapsoriasis, unspecified
0.279 0.720 0.000
L41.8 Other parapsoriasis
0.279 0.720 0.000
L41.5 Retiform parapsoriasis
0.279 0.720 0.000
L41.4 Large plaque parapsoriasis
0.279 0.720 0.000
L41.3 Small plaque parapsoriasis
0.279 0.720 0.000
L41.2 Lymphomatoid papulosis
0.279 0.720 0.000
L41.1 Pityriasis lichenoides chronica
0.279 0.720 0.000
L41.0 Pityriasis lichenoides et varioliformis acuta
0.279 0.720 0.000
L44.9 Papulosquamous disorder, unspecified
0.279 0.720 0.000
L44.8 Other specified papulosquamous disorders
0.279 0.720 0.000
L44.4 Infantile papular acrodermatitis [Giannotti-Crosti]
0.279 0.720 0.000
L44.3 Lichen ruber moniliformis
0.279 0.720 0.000
L44.2 Lichen striatus
0.279 0.720 0.000
L44.1 Lichen nitidus
0.279 0.720 0.000
L44.0 Pityriasis rubra pilaris
0.279 0.720 0.000
K51.0 Ulcerative (chronic) enterocolitis
0.276 0.724 0.000
J45.8 Mixed asthma
0.000 0.727 0.273
K51.1 Ulcerative (chronic) ileocolitis
0.261 0.739 0.000
E03.9 Hypothyroidism, unspecified
0.000 0.752 0.248
K90.4 Malabsorption due to intolerance, not elsewhere classified
0.000 0.753 0.247
E14.3 With ophthalmic complications
0.244 0.756 0.000
D69 Purpura and other haemorrhagic conditions
0.000 0.766 0.234
D69.3 Idiopathic thrombocytopenic purpura
0.000 0.776 0.224
K51.9 Ulcerative colitis, unspecified
0.213 0.787 0.000
K90.3 Pancreatic steatorrhoea
0.000 0.787 0.212
K90.2 Blind loop syndrome, not elsewhere classified
0.000 0.787 0.212
K90.1 Tropical sprue
0.000 0.787 0.212
K51.8 Other ulcerative colitis
0.212 0.788 0.000
E03 Other hypothyroidism
0.000 0.798 0.202
D69.0 Allergic purpura
0.000 0.813 0.187
E27.1 Primary adrenocortical insufficiency
0.000 0.816 0.184
D69.2 Other nonthrombocytopenic purpura
0.000 0.823 0.177
E27 Other disorders of adrenal gland
0.000 0.827 0.173
K90.8 Other intestinal malabsorption
0.000 0.830 0.169
D69.4 Other primary thrombocytopenia
0.000 0.831 0.169
D69.8 Other specified haemorrhagic conditions
0.000 0.832 0.168
E03.2 Hypothyroidism due to medicaments and other exogenous substances
0.000 0.834 0.166
D69.5 Secondary thrombocytopenia
0.000 0.839 0.161
E20-E35 Disorders of other endocrine glands
0.000 0.847 0.153
E27.2 Addisonian crisis
0.000 0.849 0.151
E00-E07 Disorders of thyroid gland
0.001 0.850 0.149
E27.4 Other and unspecified adrenocortical insufficiency
0.000 0.852 0.148
D69.1 Qualitative platelet defects
0.000 0.853 0.147
E03.5 Myxoedema coma
0.000 0.855 0.145
E03.4 Atrophy of thyroid (acquired)
0.000 0.855 0.145
E03.3 Postinfectious hypothyroidism
0.000 0.855 0.145
E03.1 Congenital hypothyroidism without goitre
0.000 0.855 0.145
E03.0 Congenital hypothyroidism with diffuse goitre
0.000 0.855 0.145
E03.8 Other specified hypothyroidism
0.000 0.855 0.145
E05 Thyrotoxicosis [hyperthyroidism]
0.000 0.857 0.143
D69.9 Haemorrhagic condition, unspecified
0.000 0.858 0.142
E05.9 Thyrotoxicosis, unspecified
0.000 0.866 0.134
E23 Hypofunction and other disorders of pituitary gland
0.000 0.872 0.128
K90.9 Intestinal malabsorption, unspecified
0.000 0.872 0.127
E20 Hypoparathyroidism
0.000 0.873 0.127
E34 Other endocrine disorders
0.000 0.873 0.126
E05.0 Thyrotoxicosis with diffuse goitre
0.000 0.874 0.126
E27.3 Drug-induced adrenocortical insufficiency
0.000 0.875 0.125
Chapter IV Endocrine, nutritional and metabolic diseases
0.004 0.875 0.121
E27.5 Adrenomedullary hyperfunction
0.000 0.876 0.124
E27.0 Other adrenocortical overactivity
0.000 0.876 0.124
E27.8 Other specified disorders of adrenal gland
0.000 0.883 0.117
E28 Ovarian dysfunction
0.000 0.885 0.115
E22 Hyperfunction of pituitary gland
0.000 0.887 0.113
E23.0 Hypopituitarism
0.000 0.889 0.111
E34.9 Endocrine disorder, unspecified
0.000 0.889 0.111
E05.8 Other thyrotoxicosis
0.000 0.890 0.110
E26 Hyperaldosteronism
0.000 0.890 0.110
E21 Hyperparathyroidism and other disorders of parathyroid gland
0.000 0.890 0.110
E35 Disorders of endocrine glands in diseases classified elsewhere
0.000 0.890 0.110
E32 Diseases of thymus
0.000 0.890 0.110
E31 Polyglandular dysfunction
0.000 0.890 0.110
E30 Disorders of puberty, not elsewhere classified
0.000 0.890 0.110
E20.9 Hypoparathyroidism, unspecified
0.000 0.891 0.109
E01 Iodine-deficiency-related thyroid disorders and allied conditions
0.001 0.892 0.107
E00 Congenital iodine-deficiency syndrome
0.001 0.892 0.107
E29 Testicular dysfunction
0.000 0.892 0.108
E05.5 Thyroid crisis or storm
0.000 0.897 0.102
E05.4 Thyrotoxicosis factitia
0.000 0.897 0.102
E05.3 Thyrotoxicosis from ectopic thyroid tissue
0.000 0.897 0.102
E05.1 Thyrotoxicosis with toxic single thyroid nodule
0.000 0.897 0.102
E27.9 Disorder of adrenal gland, unspecified
0.000 0.901 0.099
E23.7 Disorder of pituitary gland, unspecified
0.000 0.901 0.099
E02 Subclinical iodine-deficiency hypothyroidism
0.001 0.902 0.097
E25 Adrenogenital disorders
0.000 0.906 0.094
E34.0 Carcinoid syndrome
0.000 0.908 0.092
E23.3 Hypothalamic dysfunction, not elsewhere classified
0.000 0.908 0.092
E23.1 Drug-induced hypopituitarism
0.000 0.908 0.092
E22.2 Syndrome of inappropriate secretion of antidiuretic hormone
0.000 0.908 0.092
E20.8 Other hypoparathyroidism
0.000 0.908 0.091
E20.1 Pseudohypoparathyroidism
0.000 0.908 0.091
E20.0 Idiopathic hypoparathyroidism
0.000 0.908 0.091
E34.5 Androgen resistance syndrome
0.000 0.909 0.091
E34.4 Constitutional tall stature
0.000 0.909 0.091
E34.3 Short stature, not elsewhere classified
0.000 0.909 0.091
E34.2 Ectopic hormone secretion, not elsewhere classified
0.000 0.909 0.091
E34.1 Other hypersecretion of intestinal hormones
0.000 0.909 0.091
E28.3 Primary ovarian failure
0.000 0.909 0.091
E21.3 Hyperparathyroidism, unspecified
0.000 0.910 0.089
E23.2 Diabetes insipidus
0.000 0.911 0.089
E07 Other disorders of thyroid
0.001 0.913 0.086
E21.0 Primary hyperparathyroidism
0.000 0.917 0.083
E28.9 Ovarian dysfunction, unspecified
0.000 0.917 0.082
E28.8 Other ovarian dysfunction
0.000 0.917 0.082
E28.1 Androgen excess
0.000 0.917 0.082
E28.0 Oestrogen excess
0.000 0.917 0.082
E34.8 Other specified endocrine disorders
0.000 0.918 0.082
E22.9 Hyperfunction of pituitary gland, unspecified
0.000 0.919 0.081
E22.8 Other hyperfunction of pituitary gland
0.000 0.919 0.081
E23.6 Other disorders of pituitary gland
0.000 0.919 0.081
E26.0 Primary hyperaldosteronism
0.000 0.921 0.079
E26.9 Hyperaldosteronism, unspecified
0.000 0.921 0.079
E26.8 Other hyperaldosteronism
0.000 0.921 0.079
E26.1 Secondary hyperaldosteronism
0.000 0.921 0.079
E21.4 Other specified disorders of parathyroid gland
0.000 0.921 0.079
E21.2 Other hyperparathyroidism
0.000 0.921 0.079
E30.9 Disorder of puberty, unspecified
0.000 0.921 0.079
E30.8 Other disorders of puberty
0.000 0.921 0.079
E30.1 Precocious puberty
0.000 0.921 0.079
E30.0 Delayed puberty
0.000 0.921 0.079
E31.9 Polyglandular dysfunction, unspecified
0.000 0.921 0.079
E31.8 Other polyglandular dysfunction
0.000 0.921 0.079
E31.1 Polyglandular hyperfunction
0.000 0.921 0.079
E31.0 Autoimmune polyglandular failure
0.000 0.921 0.079
E32.9 Disease of thymus, unspecified
0.000 0.921 0.079
E32.8 Other diseases of thymus
0.000 0.921 0.079
E32.1 Abscess of thymus
0.000 0.921 0.079
E32.0 Persistent hyperplasia of thymus
0.000 0.921 0.079
E35.8 Disorders of other endocrine glands in diseases classified elsewhere
0.000 0.921 0.079
E35.1 Disorders of adrenal glands in diseases classified elsewhere
0.000 0.921 0.079
E35.0 Disorders of thyroid gland in diseases classified elsewhere
0.000 0.921 0.079
E24 Cushing's syndrome
0.000 0.922 0.078
E28.2 Polycystic ovarian syndrome
0.000 0.922 0.078
E21.5 Disorder of parathyroid gland, unspecified
0.000 0.922 0.078
E00.9 Congenital iodine-deficiency syndrome, unspecified
0.001 0.922 0.077
E00.2 Congenital iodine-deficiency syndrome, mixed type
0.001 0.922 0.077
E00.1 Congenital iodine-deficiency syndrome, myxoedematous type
0.001 0.922 0.077
E00.0 Congenital iodine-deficiency syndrome, neurological type
0.001 0.922 0.077
E01.8 Other iodine-deficiency-related thyroid disorders and allied conditions
0.001 0.922 0.077
E01.2 Iodine-deficiency-related (endemic) goitre, unspecified
0.001 0.922 0.077
E01.1 Iodine-deficiency-related multinodular (endemic) goitre
0.001 0.922 0.077
E01.0 Iodine-deficiency-related diffuse (endemic) goitre
0.001 0.922 0.077
E29.9 Testicular dysfunction, unspecified
0.000 0.922 0.077
E29.8 Other testicular dysfunction
0.000 0.922 0.077
E29.0 Testicular hyperfunction
0.000 0.922 0.077
E22.1 Hyperprolactinaemia
0.000 0.924 0.076
E04 Other non-toxic goitre
0.000 0.924 0.076
E29.1 Testicular hypofunction
0.000 0.925 0.075
E22.0 Acromegaly and pituitary gigantism
0.000 0.925 0.075
E15-E16 Other disorders of glucose regulation and pancreatic internal secretion
0.002 0.929 0.069
E07.8 Other specified disorders of thyroid
0.000 0.930 0.070
E05.2 Thyrotoxicosis with toxic multinodular goitre
0.000 0.930 0.070
E40-E46 Malnutrition
0.003 0.931 0.066
E65-E68 Obesity and other hyperalimentation
0.001 0.932 0.067
E25.9 Adrenogenital disorder, unspecified
0.000 0.932 0.067
E25.8 Other adrenogenital disorders
0.000 0.932 0.067
E07.1 Dyshormogenetic goitre
0.001 0.937 0.062
E07.0 Hypersecretion of calcitonin
0.001 0.937 0.062
E04.0 Non-toxic diffuse goitre
0.000 0.939 0.061
E24.2 Drug-induced Cushing's syndrome
0.000 0.940 0.059
E50-E64 Other nutritional deficiencies
0.002 0.941 0.057
E21.1 Secondary hyperparathyroidism, not elsewhere classified
0.000 0.941 0.059
E24.8 Other Cushing's syndrome
0.000 0.943 0.056
E24.4 Alcohol-induced pseudo-Cushing's syndrome
0.000 0.943 0.056
E24.3 Ectopic ACTH syndrome
0.000 0.943 0.056
E24.1 Nelson's syndrome
0.000 0.943 0.056
E06 Thyroiditis
0.001 0.944 0.055
E04.9 Non-toxic goitre, unspecified
0.000 0.945 0.055
E04.8 Other specified non-toxic goitre
0.000 0.946 0.054
E65 Localised adiposity
0.001 0.946 0.054
E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
0.001 0.949 0.051
E15 Nondiabetic hypoglycaemic coma
0.002 0.949 0.049
E44 Protein-energy malnutrition of moderate and mild degree
0.002 0.950 0.048
E45 Retarded development following protein-energy malnutrition
0.002 0.950 0.048
E43 Unspecified severe protein-energy malnutrition
0.002 0.950 0.048
E42 Marasmic kwashiorkor
0.002 0.950 0.048
E41 Nutritional marasmus
0.002 0.950 0.048
E40 Kwashiorkor
0.002 0.950 0.048
E67 Other hyperalimentation
0.001 0.951 0.048
E68 Sequelae of hyperalimentation
0.001 0.951 0.048
E11.3 With ophthalmic complications
0.048 0.952 0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
0.000 0.953 0.047
E53 Deficiency of other B group vitamins
0.001 0.954 0.045
E64 Sequelae of malnutrition and other nutritional deficiencies
0.002 0.957 0.041
E63 Other nutritional deficiencies
0.002 0.957 0.041
E56 Other vitamin deficiencies
0.002 0.957 0.041
E51 Thiamine deficiency
0.002 0.957 0.041
E50 Vitamin A deficiency
0.002 0.957 0.041
E60 Dietary zinc deficiency
0.002 0.957 0.041
E59 Dietary selenium deficiency
0.002 0.957 0.041
E54 Ascorbic acid deficiency
0.002 0.957 0.041
E52 Niacin deficiency [pellagra]
0.002 0.957 0.041
E24.0 Pituitary-dependent Cushing's disease
0.001 0.958 0.041
E24.9 Cushing's syndrome, unspecified
0.000 0.959 0.041
E06.4 Drug-induced thyroiditis
0.001 0.959 0.040
E06.2 Chronic thyroiditis with transient thyrotoxicosis
0.001 0.959 0.040
E06.0 Acute thyroiditis
0.001 0.959 0.040
E06.3 Autoimmune thyroiditis
0.000 0.960 0.040
E04.2 Non-toxic multinodular goitre
0.000 0.960 0.040
E53.8 Deficiency of other specified B group vitamins
0.000 0.961 0.039
E58 Dietary calcium deficiency
0.002 0.964 0.035
E44.1 Mild protein-energy malnutrition
0.002 0.964 0.034
E44.0 Moderate protein-energy malnutrition
0.002 0.964 0.034
E06.1 Subacute thyroiditis
0.001 0.964 0.035
E67.8 Other specified hyperalimentation
0.001 0.965 0.035
E67.3 Hypervitaminosis D
0.001 0.965 0.035
E67.2 Megavitamin-B6 syndrome
0.001 0.965 0.035
E67.1 Hypercarotenaemia
0.001 0.965 0.035
E67.0 Hypervitaminosis A
0.001 0.965 0.035
D67 Hereditary factor IX deficiency
0.000 0.966 0.034
E55 Vitamin D deficiency
0.001 0.966 0.032
E53.1 Pyridoxine deficiency
0.001 0.967 0.032
E53.0 Riboflavin deficiency
0.001 0.967 0.032
D65 Disseminated intravascular coagulation [defibrination syndrome]
0.000 0.967 0.033
E16 Other disorders of pancreatic internal secretion
0.001 0.968 0.031
E61 Deficiency of other nutrient elements
0.002 0.969 0.030
E06.5 Other chronic thyroiditis
0.001 0.969 0.030
E50.9 Vitamin A deficiency, unspecified
0.001 0.969 0.030
E50.8 Other manifestations of vitamin A deficiency
0.001 0.969 0.030
E50.7 Other ocular manifestations of vitamin A deficiency
0.001 0.969 0.030
E50.6 Vitamin A deficiency with xerophthalmic scars of cornea
0.001 0.969 0.030
E50.5 Vitamin A deficiency with night blindness
0.001 0.969 0.030
E50.4 Vitamin A deficiency with keratomalacia
0.001 0.969 0.030
E50.3 Vitamin A deficiency with corneal ulceration and xerosis
0.001 0.969 0.030
E50.2 Vitamin A deficiency with corneal xerosis
0.001 0.969 0.030
E50.1 Vitamin A deficiency with Bitot's spot and conjunctival xerosis
0.001 0.969 0.030
E50.0 Vitamin A deficiency with conjunctival xerosis
0.001 0.969 0.030
E51.9 Thiamine deficiency, unspecified
0.001 0.969 0.030
E51.8 Other manifestations of thiamine deficiency
0.001 0.969 0.030
E51.2 Wernicke's encephalopathy
0.001 0.969 0.030
E51.1 Beriberi
0.001 0.969 0.030
E56.9 Vitamin deficiency, unspecified
0.001 0.969 0.030
E56.8 Deficiency of other vitamins
0.001 0.969 0.030
E56.1 Deficiency of vitamin K
0.001 0.969 0.030
E56.0 Deficiency of vitamin E
0.001 0.969 0.030
E63.9 Nutritional deficiency, unspecified
0.001 0.969 0.030
E63.8 Other specified nutritional deficiencies
0.001 0.969 0.030
E63.1 Imbalance of constituents of food intake
0.001 0.969 0.030
E63.0 Essential fatty acid [EFA] deficiency
0.001 0.969 0.030
E64.9 Sequelae of unspecified nutritional deficiency
0.001 0.969 0.030
E64.8 Sequelae of other nutritional deficiencies
0.001 0.969 0.030
E64.3 Sequelae of rickets
0.001 0.969 0.030
E64.2 Sequelae of vitamin C deficiency
0.001 0.969 0.030
E64.1 Sequelae of vitamin A deficiency
0.001 0.969 0.030
E64.0 Sequelae of protein-energy malnutrition
0.001 0.969 0.030
E46 Unspecified protein-energy malnutrition
0.003 0.971 0.027
H43.3 Other vitreous opacities
0.029 0.971 0.000
H43.8 Other disorders of vitreous body
0.029 0.971 0.000
H43 Disorders of vitreous body
0.028 0.972 0.000
E04.1 Non-toxic single thyroid nodule
0.000 0.973 0.027
E53.9 Vitamin B deficiency, unspecified
0.001 0.973 0.026
D86 Sarcoidosis
0.000 0.973 0.027
D80-D89 Certain disorders involving the immune mechanism
0.000 0.974 0.026
H43.1 Vitreous haemorrhage
0.026 0.974 0.000
D86.9 Sarcoidosis, unspecified
0.000 0.974 0.026
D66 Hereditary factor VIII deficiency
0.000 0.975 0.025
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
0.000 0.975 0.025
Q38.7 Pharyngeal pouch
0.025 0.975 0.000
E06.9 Thyroiditis, unspecified
0.001 0.975 0.023
E55.0 Rickets, active
0.001 0.976 0.023
E16.1 Other hypoglycaemia
0.001 0.976 0.024
D80 Immunodeficiency with predominantly antibody defects
0.000 0.976 0.024
D86.0 Sarcoidosis of lung
0.000 0.976 0.024
E16.9 Disorder of pancreatic internal secretion, unspecified
0.001 0.976 0.023
E16.8 Other specified disorders of pancreatic internal secretion
0.001 0.976 0.023
E16.4 Abnormal secretion of gastrin
0.001 0.976 0.023
E16.3 Increased secretion of glucagon
0.001 0.976 0.023
E61.9 Deficiency of nutrient element, unspecified
0.001 0.977 0.021
E61.8 Deficiency of other specified nutrient elements
0.001 0.977 0.021
E61.7 Deficiency of multiple nutrient elements
0.001 0.977 0.021
E61.6 Vanadium deficiency
0.001 0.977 0.021
E61.5 Molybdenum deficiency
0.001 0.977 0.021
E61.4 Chromium deficiency
0.001 0.977 0.021
E61.3 Manganese deficiency
0.001 0.977 0.021
E61.0 Copper deficiency
0.001 0.977 0.021
Q61 Cystic kidney disease
0.022 0.978 0.000
D80.1 Nonfamilial hypogammaglobulinaemia
0.000 0.978 0.022
Q61.0 Congenital single renal cyst
0.022 0.978 0.000
D86.1 Sarcoidosis of lymph nodes
0.000 0.979 0.021
E07.9 Disorder of thyroid, unspecified
0.001 0.979 0.020
Q38 Other congenital malformations of tongue, mouth and pharynx
0.021 0.979 0.000
D84 Other immunodeficiencies
0.000 0.980 0.020
D86.3 Sarcoidosis of skin
0.000 0.980 0.020
H43.0 Vitreous prolapse
0.020 0.980 0.000
Q61.2 Polycystic kidney, adult type
0.020 0.980 0.000
E16.0 Drug-induced hypoglycaemia without coma
0.001 0.980 0.019
D83 Common variable immunodeficiency
0.000 0.980 0.019
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.000 0.981 0.019
H43.9 Disorder of vitreous body, unspecified
0.019 0.981 0.000
D82 Immunodeficiency associated with other major defects
0.000 0.981 0.019
D81 Combined immunodeficiencies
0.000 0.981 0.019
E61.2 Magnesium deficiency
0.002 0.981 0.018
D70-D77 Other diseases of blood and blood-forming organs
0.000 0.981 0.019
Q61.3 Polycystic kidney, unspecified
0.019 0.981 0.000
E14.9 Without complications
0.019 0.981 0.000
D73 Diseases of spleen
0.000 0.981 0.019
D80.2 Selective deficiency of immunoglobulin A [IgA]
0.000 0.982 0.018
K90-K93 Other diseases of the digestive system
0.000 0.982 0.018
D73.0 Hyposplenism
0.000 0.982 0.018
Q61.4 Renal dysplasia
0.017 0.983 0.000
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.000 0.983 0.017
D80.8 Other immunodeficiencies with predominantly antibody defects
0.000 0.983 0.017
D80.7 Transient hypogammaglobulinaemia of infancy
0.000 0.983 0.017
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
0.000 0.983 0.017
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]
0.000 0.983 0.017
D80.4 Selective deficiency of immunoglobulin M [IgM]
0.000 0.983 0.017
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses
0.000 0.983 0.017
D80.0 Hereditary hypogammaglobulinaemia
0.000 0.983 0.017
D73.5 Infarction of spleen
0.000 0.983 0.017
H43.2 Crystalline deposits in vitreous body
0.017 0.983 0.000
E61.1 Iron deficiency
0.001 0.983 0.016
Q38-Q45 Other congenital malformations of the digestive system
0.017 0.983 0.000
R31 Unspecified haematuria
0.017 0.983 0.000
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.000 0.984 0.016
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.016 0.984 0.000
Q61.5 Medullary cystic kidney
0.016 0.984 0.000
Q60-Q64 Congenital malformations of the urinary system
0.016 0.984 0.000
D84.9 Immunodeficiency, unspecified
0.000 0.984 0.016
D55-D59 Haemolytic anaemias
0.000 0.984 0.016
Q38.1 Ankyloglossia
0.016 0.984 0.000
Q61.9 Cystic kidney disease, unspecified
0.016 0.984 0.000
Q61.8 Other cystic kidney diseases
0.016 0.984 0.000
Q61.1 Polycystic kidney, infantile type
0.016 0.984 0.000
Q80-Q89 Other congenital malformations
0.016 0.984 0.000
E55.9 Vitamin D deficiency, unspecified
0.001 0.985 0.015
Q38.8 Other congenital malformations of pharynx
0.015 0.985 0.000
Q38.6 Other congenital malformations of mouth
0.015 0.985 0.000
Q38.5 Congenital malformations of palate, not elsewhere classified
0.015 0.985 0.000
Q38.4 Congenital malformations of salivary glands and ducts
0.015 0.985 0.000
Q38.3 Other congenital malformations of tongue
0.015 0.985 0.000
Q38.2 Macroglossia
0.015 0.985 0.000
Q38.0 Congenital malformations of lips, not elsewhere classified
0.015 0.985 0.000
D84.8 Other specified immunodeficiencies
0.000 0.985 0.015
D84.1 Defects in the complement system
0.000 0.985 0.015
D84.0 Lymphocyte function antigen-1 [LFA-1] defect
0.000 0.985 0.015
D72 Other disorders of white blood cells
0.000 0.985 0.015
D83.9 Common variable immunodeficiency, unspecified
0.000 0.985 0.014
D73.8 Other diseases of spleen
0.000 0.985 0.014
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
0.000 0.986 0.014
D83.8 Other common variable immunodeficiencies
0.000 0.986 0.014
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells
0.000 0.986 0.014
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
0.000 0.986 0.014
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
0.000 0.986 0.014
Q85 Phakomatoses, not elsewhere classified
0.014 0.986 0.000
D86.8 Sarcoidosis of other and combined sites
0.000 0.986 0.014
D81.9 Combined immunodeficiency, unspecified
0.000 0.986 0.014
D81.8 Other combined immunodeficiencies
0.000 0.986 0.014
D81.7 Major histocompatibility complex class II deficiency
0.000 0.986 0.014
D81.6 Major histocompatibility complex class I deficiency
0.000 0.986 0.014
D81.5 Purine nucleoside phosphorylase [PNP] deficiency
0.000 0.986 0.014
D81.4 Nezelof's syndrome
0.000 0.986 0.014
D81.3 Adenosine deaminase [ADA] deficiency
0.000 0.986 0.014
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
0.000 0.986 0.014
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
0.000 0.986 0.014
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
0.000 0.986 0.014
D82.9 Immunodeficiency associated with major defect, unspecified
0.000 0.986 0.014
D82.8 Immunodeficiency associated with other specified major defects
0.000 0.986 0.014
D82.4 Hyperimmunoglobulin E [IgE] syndrome
0.000 0.986 0.014
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
0.000 0.986 0.014
D82.2 Immunodeficiency with short-limbed stature
0.000 0.986 0.014
D82.1 Di George's syndrome
0.000 0.986 0.014
D82.0 Wiskott-Aldrich syndrome
0.000 0.986 0.014
Q40 Other congenital malformations of upper alimentary tract
0.014 0.986 0.000
D74 Methaemoglobinaemia
0.000 0.986 0.014
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
0.000 0.986 0.014
D71 Functional disorders of polymorphonuclear neutrophils
0.000 0.986 0.014
D73.9 Disease of spleen, unspecified
0.000 0.986 0.014
D73.2 Chronic congestive splenomegaly
0.000 0.986 0.014
D73.1 Hypersplenism
0.000 0.986 0.014
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.014 0.986 0.000
Q83 Congenital malformations of breast
0.014 0.986 0.000
K93 Disorders of other digestive organs in diseases classified elsewhere
0.000 0.987 0.013
D59 Acquired haemolytic anaemia
0.000 0.987 0.013
Q20-Q28 Congenital malformations of the circulatory system
0.013 0.987 0.000
D73.3 Abscess of spleen
0.000 0.987 0.013
Q65 Congenital deformities of hip
0.013 0.987 0.000
Q35-Q37 Cleft lip and cleft palate
0.012 0.987 0.000
Q45 Other congenital malformations of digestive system
0.012 0.988 0.000
Q42 Congenital absence, atresia and stenosis of large intestine
0.012 0.988 0.000
Q41 Congenital absence, atresia and stenosis of small intestine
0.012 0.988 0.000
D73.4 Cyst of spleen
0.000 0.988 0.012
E66 Obesity
0.000 0.988 0.012
Q83.1 Accessory breast
0.012 0.988 0.000
D89.9 Disorder involving the immune mechanism, unspecified
0.000 0.988 0.012
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.012 0.988 0.000
Q89 Other congenital malformations, not elsewhere classified
0.012 0.988 0.000
Q85.0 Neurofibromatosis (nonmalignant)
0.012 0.988 0.000
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified
0.000 0.988 0.012
D89.3 Immune reconstitution syndrome
0.000 0.988 0.012
D89.1 Cryoglobulinaemia
0.000 0.988 0.012
Q30-Q34 Congenital malformations of the respiratory system
0.012 0.988 0.000
D89.0 Polyclonal hypergammaglobulinaemia
0.000 0.988 0.012
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.012 0.988 0.000
D57 Sickle-cell disorders
0.000 0.988 0.012
D55 Anaemia due to enzyme disorders
0.000 0.988 0.012
Q85.1 Tuberous sclerosis
0.012 0.988 0.000
D56 Thalassaemia
0.000 0.988 0.012
Q40.3 Congenital malformation of stomach, unspecified
0.012 0.988 0.000
Q39 Congenital malformations of oesophagus
0.012 0.988 0.000
Q00-Q07 Congenital malformations of the nervous system
0.012 0.988 0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
0.011 0.989 0.000
Q84 Other congenital malformations of integument
0.011 0.989 0.000
Q81 Epidermolysis bullosa
0.011 0.989 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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