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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

rs855791
log Bayes Factor = 4.53368
Chromosome 22   position 37,462,936  (GRCh37) Explore rs855791 on Ensembl!
Variant rs855791 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
  
D64.9 Anaemia, unspecified
0.000 0.000 1.000
D64 Other anaemias
0.000 0.156 0.844
D60-D64 Aplastic and other anaemias
0.000 0.215 0.785
D62 Acute posthaemorrhagic anaemia
0.000 0.215 0.785
D64.4 Congenital dyserythropoietic anaemia
0.000 0.395 0.605
D64.2 Secondary sideroblastic anaemia due to drugs and toxins
0.000 0.395 0.605
D64.1 Secondary sideroblastic anaemia due to disease
0.000 0.395 0.605
D64.0 Hereditary sideroblastic anaemia
0.000 0.429 0.571
D64.3 Other sideroblastic anaemias
0.000 0.429 0.570
D60 Acquired pure red cell aplasia [erythroblastopenia]
0.000 0.485 0.515
D64.8 Other specified anaemias
0.000 0.500 0.500
D61 Other aplastic anaemias
0.000 0.595 0.405
D60.8 Other acquired pure red cell aplasias
0.000 0.631 0.369
D60.1 Transient acquired pure red cell aplasia
0.000 0.631 0.369
D60.0 Chronic acquired pure red cell aplasia
0.000 0.631 0.369
D60.9 Acquired pure red cell aplasia, unspecified
0.000 0.679 0.321
D61.1 Drug-induced aplastic anaemia
0.000 0.701 0.299
D61.8 Other specified aplastic anaemias
0.000 0.709 0.291
D61.3 Idiopathic aplastic anaemia
0.000 0.709 0.291
D61.2 Aplastic anaemia due to other external agents
0.000 0.709 0.291
D63 Anaemia in chronic diseases classified elsewhere
0.000 0.711 0.289
E83.1 Disorders of iron metabolism
0.272 0.728 0.000
D61.0 Constitutional aplastic anaemia
0.000 0.740 0.260
D12 Benign neoplasm of colon, rectum, anus and anal canal
0.209 0.791 0.000
D63.1 Anaemia in other chronic diseases classified elsewhere
0.000 0.793 0.207
D12.2 Ascending colon
0.204 0.796 0.000
D12.0 Caecum
0.201 0.799 0.000
D12.7 Rectosigmoid junction
0.199 0.801 0.000
D12.4 Descending colon
0.197 0.803 0.000
D12.8 Rectum
0.197 0.803 0.000
D12.3 Transverse colon
0.184 0.816 0.000
D61.9 Aplastic anaemia, unspecified
0.000 0.826 0.173
D12.1 Appendix
0.152 0.848 0.000
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
0.000 0.868 0.132
D63.0 Anaemia in neoplastic disease
0.000 0.872 0.128
D50-D53 Nutritional anaemias
0.000 0.884 0.116
D55-D59 Haemolytic anaemias
0.000 0.889 0.111
D12.9 Anus and anal canal
0.110 0.890 0.000
D63.8 Anaemia in other chronic diseases classified elsewhere
0.000 0.893 0.107
D50 Iron deficiency anaemia
0.000 0.898 0.102
D50.8 Other iron deficiency anaemias
0.000 0.899 0.101
D51 Vitamin B12 deficiency anaemia
0.000 0.900 0.100
E83 Disorders of mineral metabolism
0.097 0.903 0.000
D12.5 Sigmoid colon
0.095 0.905 0.000
D59 Acquired haemolytic anaemia
0.000 0.906 0.094
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
0.000 0.908 0.092
D59.1 Other autoimmune haemolytic anaemias
0.000 0.913 0.086
D57 Sickle-cell disorders
0.000 0.914 0.086
D53 Other nutritional anaemias
0.000 0.916 0.084
D55 Anaemia due to enzyme disorders
0.000 0.920 0.079
D56 Thalassaemia
0.000 0.923 0.077
D51.3 Other dietary vitamin B12 deficiency anaemia
0.000 0.923 0.077
D58 Other hereditary haemolytic anaemias
0.000 0.924 0.076
E83.4 Disorders of magnesium metabolism
0.075 0.925 0.000
E83.9 Disorder of mineral metabolism, unspecified
0.074 0.926 0.000
D50.1 Sideropenic dysphagia
0.000 0.927 0.072
D59.0 Drug-induced autoimmune haemolytic anaemia
0.000 0.928 0.072
D51.2 Transcobalamin II deficiency
0.000 0.928 0.072
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria
0.000 0.928 0.072
D51.8 Other vitamin B12 deficiency anaemias
0.000 0.929 0.071
E83.8 Other disorders of mineral metabolism
0.069 0.930 0.000
E83.2 Disorders of zinc metabolism
0.069 0.930 0.000
E83.0 Disorders of copper metabolism
0.069 0.930 0.000
D57.1 Sickle-cell anaemia without crisis
0.000 0.931 0.069
D59.8 Other acquired haemolytic anaemias
0.000 0.932 0.067
D59.6 Haemoglobinuria due to haemolysis from other external causes
0.000 0.932 0.067
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
0.000 0.932 0.067
D59.3 Haemolytic-uraemic syndrome
0.000 0.932 0.067
D59.2 Drug-induced nonautoimmune haemolytic anaemia
0.000 0.932 0.067
D59.4 Other nonautoimmune haemolytic anaemias
0.000 0.934 0.066
D53.1 Other megaloblastic anaemias, not elsewhere classified
0.000 0.936 0.064
D52 Folate deficiency anaemia
0.000 0.937 0.063
D57.8 Other sickle-cell disorders
0.000 0.938 0.062
D57.3 Sickle-cell trait
0.000 0.938 0.062
D57.2 Double heterozygous sickling disorders
0.000 0.938 0.062
D57.0 Sickle-cell anaemia with crisis
0.000 0.938 0.062
D80-D89 Certain disorders involving the immune mechanism
0.000 0.938 0.062
D58.0 Hereditary spherocytosis
0.000 0.939 0.061
E83.5 Disorders of calcium metabolism
0.061 0.939 0.000
D53.8 Other specified nutritional anaemias
0.000 0.939 0.060
D53.2 Scorbutic anaemia
0.000 0.939 0.060
D53.0 Protein deficiency anaemia
0.000 0.939 0.060
D55.9 Anaemia due to enzyme disorder, unspecified
0.000 0.943 0.057
D55.8 Other anaemias due to enzyme disorders
0.000 0.943 0.057
D55.3 Anaemia due to disorders of nucleotide metabolism
0.000 0.943 0.057
D55.2 Anaemia due to disorders of glycolytic enzymes
0.000 0.943 0.057
D55.1 Anaemia due to other disorders of glutathione metabolism
0.000 0.943 0.057
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
0.000 0.943 0.057
D53.9 Nutritional anaemia, unspecified
0.000 0.943 0.057
D56.9 Thalassaemia, unspecified
0.000 0.944 0.055
D56.8 Other thalassaemias
0.000 0.944 0.055
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]
0.000 0.944 0.055
D56.2 Delta-beta thalassaemia
0.000 0.944 0.055
D56.0 Alpha thalassaemia
0.000 0.944 0.055
D51.9 Vitamin B12 deficiency anaemia, unspecified
0.000 0.944 0.056
D56.3 Thalassaemia trait
0.000 0.945 0.055
D58.8 Other specified hereditary haemolytic anaemias
0.000 0.945 0.054
D58.1 Hereditary elliptocytosis
0.000 0.945 0.054
D56.1 Beta thalassaemia
0.000 0.946 0.054
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)
0.000 0.947 0.053
D58.9 Hereditary haemolytic anaemia, unspecified
0.000 0.949 0.051
D59.9 Acquired haemolytic anaemia, unspecified
0.000 0.953 0.047
D82 Immunodeficiency associated with other major defects
0.000 0.953 0.047
E80.4 Gilbert's syndrome
0.046 0.954 0.000
D58.2 Other haemoglobinopathies
0.000 0.955 0.045
D52.8 Other folate deficiency anaemias
0.000 0.955 0.045
D52.1 Drug-induced folate deficiency anaemia
0.000 0.955 0.045
D52.0 Dietary folate deficiency anaemia
0.000 0.955 0.045
D81 Combined immunodeficiencies
0.000 0.956 0.044
D80 Immunodeficiency with predominantly antibody defects
0.000 0.958 0.042
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.000 0.958 0.042
D86 Sarcoidosis
0.000 0.958 0.042
E80 Disorders of porphyrin and bilirubin metabolism
0.039 0.961 0.000
D86.3 Sarcoidosis of skin
0.000 0.963 0.037
E83.3 Disorders of phosphorus metabolism
0.037 0.963 0.000
D83 Common variable immunodeficiency
0.000 0.963 0.036
D82.1 Di George's syndrome
0.000 0.964 0.036
D86.8 Sarcoidosis of other and combined sites
0.000 0.964 0.036
D50.9 Iron deficiency anaemia, unspecified
0.000 0.964 0.036
D89.9 Disorder involving the immune mechanism, unspecified
0.000 0.964 0.036
D89.1 Cryoglobulinaemia
0.000 0.964 0.035
D80.2 Selective deficiency of immunoglobulin A [IgA]
0.000 0.965 0.034
D82.9 Immunodeficiency associated with major defect, unspecified
0.000 0.966 0.034
D82.8 Immunodeficiency associated with other specified major defects
0.000 0.966 0.034
D82.4 Hyperimmunoglobulin E [IgE] syndrome
0.000 0.966 0.034
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
0.000 0.966 0.034
D82.2 Immunodeficiency with short-limbed stature
0.000 0.966 0.034
D82.0 Wiskott-Aldrich syndrome
0.000 0.966 0.034
D80.4 Selective deficiency of immunoglobulin M [IgM]
0.000 0.967 0.033
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.000 0.967 0.033
E80.2 Other porphyria
0.032 0.967 0.000
D84 Other immunodeficiencies
0.000 0.968 0.032
D81.9 Combined immunodeficiency, unspecified
0.000 0.968 0.032
D81.8 Other combined immunodeficiencies
0.000 0.968 0.032
D81.7 Major histocompatibility complex class II deficiency
0.000 0.968 0.032
D81.6 Major histocompatibility complex class I deficiency
0.000 0.968 0.032
D81.5 Purine nucleoside phosphorylase [PNP] deficiency
0.000 0.968 0.032
D81.4 Nezelof's syndrome
0.000 0.968 0.032
D81.3 Adenosine deaminase [ADA] deficiency
0.000 0.968 0.032
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
0.000 0.968 0.032
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
0.000 0.968 0.032
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
0.000 0.968 0.032
D70-D77 Other diseases of blood and blood-forming organs
0.000 0.968 0.032
E70-E90 Metabolic disorders
0.032 0.968 0.000
E80.1 Porphyria cutanea tarda
0.031 0.969 0.000
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
0.000 0.969 0.031
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.000 0.969 0.031
D80.8 Other immunodeficiencies with predominantly antibody defects
0.000 0.969 0.031
D80.7 Transient hypogammaglobulinaemia of infancy
0.000 0.969 0.031
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
0.000 0.969 0.031
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]
0.000 0.969 0.031
D80.0 Hereditary hypogammaglobulinaemia
0.000 0.969 0.031
D89.3 Immune reconstitution syndrome
0.000 0.969 0.030
D86.1 Sarcoidosis of lymph nodes
0.000 0.969 0.031
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified
0.000 0.970 0.030
Z45.8 Adjustment and management of other implanted devices
0.030 0.970 0.000
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses
0.000 0.971 0.028
E80.7 Disorder of bilirubin metabolism, unspecified
0.028 0.972 0.000
E80.5 Crigler-Najjar syndrome
0.028 0.972 0.000
E80.3 Defects of catalase and peroxydase
0.028 0.972 0.000
E80.0 Hereditary erythropoietic porphyria
0.028 0.972 0.000
D89.0 Polyclonal hypergammaglobulinaemia
0.000 0.973 0.027
D83.8 Other common variable immunodeficiencies
0.000 0.974 0.026
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells
0.000 0.974 0.026
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
0.000 0.974 0.026
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
0.000 0.974 0.026
D12.6 Colon, unspecified
0.026 0.974 0.000
E84 Cystic fibrosis
0.026 0.974 0.000
M62.80 Other specified disorders of muscle (Multiple sites)
0.000 0.974 0.026
E72 Other disorders of amino-acid metabolism
0.025 0.975 0.000
E70 Disorders of aromatic amino-acid metabolism
0.025 0.975 0.000
D75 Other diseases of blood and blood-forming organs
0.000 0.975 0.025
D52.9 Folate deficiency anaemia, unspecified
0.000 0.976 0.024
E80.6 Other disorders of bilirubin metabolism
0.024 0.976 0.000
E75 Disorders of sphingolipid metabolism and other lipid storage disorders
0.024 0.976 0.000
D66 Hereditary factor VIII deficiency
0.000 0.976 0.024
M62.8 Other specified disorders of muscle
0.000 0.976 0.024
D84.0 Lymphocyte function antigen-1 [LFA-1] defect
0.000 0.977 0.023
D74 Methaemoglobinaemia
0.000 0.977 0.023
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
0.000 0.977 0.023
D71 Functional disorders of polymorphonuclear neutrophils
0.000 0.977 0.023
E73 Lactose intolerance
0.023 0.977 0.000
E77 Disorders of glycoprotein metabolism
0.023 0.977 0.000
E76 Disorders of glycosaminoglycan metabolism
0.023 0.977 0.000
E71 Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism
0.023 0.977 0.000
E90 Nutritional and metabolic disorders in diseases classified elsewhere
0.023 0.977 0.000
E74 Other disorders of carbohydrate metabolism
0.022 0.977 0.000
E85 Amyloidosis
0.022 0.978 0.000
D84.8 Other specified immunodeficiencies
0.000 0.978 0.022
E79 Disorders of purine and pyrimidine metabolism
0.022 0.978 0.000
D67 Hereditary factor IX deficiency
0.000 0.978 0.022
D73 Diseases of spleen
0.000 0.978 0.022
E84.0 Cystic fibrosis with pulmonary manifestations
0.022 0.978 0.000
M62.86 Other specified disorders of muscle (Lower leg)
0.000 0.979 0.021
D80.1 Nonfamilial hypogammaglobulinaemia
0.000 0.979 0.021
D75.9 Disease of blood and blood-forming organs, unspecified
0.000 0.979 0.021
E72.0 Disorders of amino-acid transport
0.021 0.979 0.000
D84.1 Defects in the complement system
0.000 0.979 0.020
M62.85 Other specified disorders of muscle (Pelvic region and thigh)
0.000 0.979 0.020
E70.3 Albinism
0.020 0.980 0.000
E84.9 Cystic fibrosis, unspecified
0.020 0.980 0.000
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
0.000 0.980 0.020
M62.83 Other specified disorders of muscle (Forearm)
0.000 0.980 0.020
D75.1 Secondary polycythaemia
0.000 0.980 0.020
O42.1 Premature rupture of membranes, onset of labour after 24 hours
0.000 0.980 0.020
M62.89 Other specified disorders of muscle (Site unspecified)
0.000 0.981 0.019
E75.5 Other lipid storage disorders
0.019 0.981 0.000
E84.8 Cystic fibrosis with other manifestations
0.019 0.981 0.000
E84.1 Cystic fibrosis with intestinal manifestations
0.019 0.981 0.000
M62.82 Other specified disorders of muscle (Upper arm)
0.000 0.981 0.019
E85.9 Amyloidosis, unspecified
0.019 0.981 0.000
D83.9 Common variable immunodeficiency, unspecified
0.001 0.981 0.018
M62.84 Other specified disorders of muscle (Hand)
0.000 0.981 0.018
E72.9 Disorder of amino-acid metabolism, unspecified
0.018 0.982 0.000
E72.8 Other specified disorders of amino-acid metabolism
0.018 0.982 0.000
E72.5 Disorders of glycine metabolism
0.018 0.982 0.000
E72.4 Disorders of ornithine metabolism
0.018 0.982 0.000
E72.3 Disorders of lysine and hydroxylysine metabolism
0.018 0.982 0.000
E72.2 Disorders of urea cycle metabolism
0.018 0.982 0.000
E72.1 Disorders of sulphur-bearing amino-acid metabolism
0.018 0.982 0.000
E70.9 Disorder of aromatic amino-acid metabolism, unspecified
0.018 0.982 0.000
E70.8 Other disorders of aromatic amino-acid metabolism
0.018 0.982 0.000
E70.2 Disorders of tyrosine metabolism
0.018 0.982 0.000
E70.1 Other hyperphenylalaninaemias
0.018 0.982 0.000
E70.0 Classical phenylketonuria
0.018 0.982 0.000
D75.0 Familial erythrocytosis
0.000 0.982 0.018
D73.3 Abscess of spleen
0.000 0.982 0.018
D84.9 Immunodeficiency, unspecified
0.000 0.982 0.017
D75.2 Essential thrombocytosis
0.000 0.982 0.017
E75.6 Lipid storage disorder, unspecified
0.017 0.983 0.000
E75.4 Neuronal ceroid lipofuscinosis
0.017 0.983 0.000
E75.3 Sphingolipidosis, unspecified
0.017 0.983 0.000
E75.1 Other gangliosidosis
0.017 0.983 0.000
E75.0 GM2 gangliosidosis
0.017 0.983 0.000
M62.87 Other specified disorders of muscle (Ankle and foot)
0.000 0.983 0.017
E85.8 Other amyloidosis
0.017 0.983 0.000
E74.3 Other disorders of intestinal carbohydrate absorption
0.017 0.983 0.000
D74.9 Methaemoglobinaemia, unspecified
0.000 0.983 0.017
D74.8 Other methaemoglobinaemias
0.000 0.983 0.017
D74.0 Congenital methaemoglobinaemia
0.000 0.983 0.017
E73.9 Lactose intolerance, unspecified
0.017 0.983 0.000
E73.8 Other lactose intolerance
0.017 0.983 0.000
E73.1 Secondary lactase deficiency
0.017 0.983 0.000
E73.0 Congenital lactase deficiency
0.017 0.983 0.000
E71.3 Disorders of fatty-acid metabolism
0.017 0.983 0.000
E71.2 Disorder of branched-chain amino-acid metabolism, unspecified
0.017 0.983 0.000
E71.1 Other disorders of branched-chain amino-acid metabolism
0.017 0.983 0.000
E71.0 Maple-syrup-urine disease
0.017 0.983 0.000
E76.9 Disorder of glucosaminoglycan metabolism, unspecified
0.017 0.983 0.000
E76.8 Other disorders of glucosaminoglycan metabolism
0.017 0.983 0.000
E76.3 Mucopolysaccharidosis, unspecified
0.017 0.983 0.000
E76.2 Other mucopolysaccharidoses
0.017 0.983 0.000
E76.1 Mucopolysaccharidosis, type II
0.017 0.983 0.000
E76.0 Mucopolysaccharidosis, type I
0.017 0.983 0.000
E77.9 Disorder of glycoprotein metabolism, unspecified
0.017 0.983 0.000
E77.8 Other disorders of glycoprotein metabolism
0.017 0.983 0.000
E77.1 Defects in glycoprotein degradation
0.017 0.983 0.000
E77.0 Defects in posttranslational modification of lysosomal enzymes
0.017 0.983 0.000
E74.9 Disorder of carbohydrate metabolism, unspecified
0.016 0.984 0.000
E74.8 Other specified disorders of carbohydrate metabolism
0.016 0.984 0.000
E74.4 Disorders of pyruvate metabolism and gluconeogenesis
0.016 0.984 0.000
E74.2 Disorders of galactose metabolism
0.016 0.984 0.000
E74.1 Disorders of fructose metabolism
0.016 0.984 0.000
E85.3 Secondary systemic amyloidosis
0.016 0.984 0.000
D73.8 Other diseases of spleen
0.000 0.984 0.016
E75.2 Other sphingolipidosis
0.016 0.984 0.000
E79.9 Disorder of purine and pyrimidine metabolism, unspecified
0.016 0.984 0.000
E79.8 Other disorders of purine and pyrimidine metabolism
0.016 0.984 0.000
E79.1 Lesch-Nyhan syndrome
0.016 0.984 0.000
E85.2 Heredofamilial amyloidosis, unspecified
0.016 0.984 0.000
E85.1 Neuropathic heredofamilial amyloidosis
0.016 0.984 0.000
E85.0 Nonneuropathic heredofamilial amyloidosis
0.016 0.984 0.000
D73.4 Cyst of spleen
0.000 0.984 0.016
D73.2 Chronic congestive splenomegaly
0.000 0.984 0.016
D73.9 Disease of spleen, unspecified
0.000 0.984 0.016
U80.8 Agent resistant to other penicillin-related antibiotic
0.000 0.984 0.016
D73.0 Hyposplenism
0.000 0.984 0.016
E79.0 Hyperuricaemia without signs of inflammatory arthritis and tophaceous disease
0.015 0.984 0.000
E74.0 Glycogen storage disease
0.015 0.985 0.000
D75.8 Other specified diseases of blood and blood-forming organs
0.000 0.985 0.015
O42 Premature rupture of membranes
0.000 0.985 0.015
D65 Disseminated intravascular coagulation [defibrination syndrome]
0.000 0.985 0.014
D76.2 Haemophagocytic syndrome, infection-associated
0.000 0.985 0.014
D76.1 Haemophagocytic lymphohistiocytosis
0.000 0.985 0.014
D76.0 Langerhans' cell histiocytosis, not elsewhere classified
0.000 0.985 0.014
D72 Other disorders of white blood cells
0.000 0.986 0.014
M62.88 Other specified disorders of muscle (Other)
0.000 0.986 0.014
D73.5 Infarction of spleen
0.000 0.986 0.014
D73.1 Hypersplenism
0.000 0.986 0.014
E89 Postprocedural endocrine and metabolic disorders, not elsewhere classified
0.014 0.986 0.000
O42.9 Premature rupture of membranes, unspecified
0.000 0.987 0.013
M62.81 Other specified disorders of muscle (Shoulder region)
0.000 0.987 0.013
D68 Other coagulation defects
0.000 0.987 0.013
R07.4 Chest pain, unspecified
0.000 0.987 0.013
D86.0 Sarcoidosis of lung
0.000 0.987 0.012
D68.6 Other Thrombophilia
0.000 0.988 0.012
O42.0 Premature rupture of membranes, onset of labour within 24 hours
0.000 0.988 0.012
Z01.6 Radiological examination, not elsewhere classified
0.012 0.988 0.000
O42.2 Premature rupture of membranes, labour delayed by therapy
0.000 0.988 0.012
E89.3 Postprocedural hypopituitarism
0.011 0.988 0.000
D76.3 Other histiocytosis syndromes
0.000 0.989 0.011
E89.6 Postprocedural adrenocortical(-medullary) hypofunction
0.011 0.989 0.000
C56 Malignant neoplasm of ovary
0.011 0.989 0.000
D89.2 Hypergammaglobulinaemia, unspecified
0.000 0.989 0.011
N75.0 Cyst of Bartholin's gland
0.000 0.989 0.011
U80 Agent resistant to penicillin and related antibiotics
0.000 0.989 0.011
D68.5 Primary Thrombophilia
0.000 0.989 0.011
E88 Other metabolic disorders
0.011 0.989 0.000
D72.9 Disorder of white blood cells, unspecified
0.000 0.989 0.010
D72.0 Genetic anomalies of leukocytes
0.000 0.989 0.010
E89.8 Other postprocedural endocrine and metabolic disorders
0.010 0.990 0.000
M62 Other disorders of muscle
0.000 0.990 0.010
E89.9 Postprocedural endocrine and metabolic disorder, unspecified
0.010 0.990 0.000
E89.5 Postprocedural testicular hypofunction
0.010 0.990 0.000
E89.1 Postprocedural hypoinsulinaemia
0.010 0.990 0.000
D86.9 Sarcoidosis, unspecified
0.000 0.990 0.010
E85.4 Organ-limited amyloidosis
0.009 0.990 0.000
D72.1 Eosinophilia
0.000 0.990 0.009
D68.3 Haemorrhagic disorder due to circulating anticoagulants
0.000 0.991 0.009
D68.4 Acquired coagulation factor deficiency
0.000 0.991 0.009
U80.1 Methicillin resistant agent
0.000 0.991 0.009
D68.1 Hereditary factor XI deficiency
0.000 0.991 0.009
K76.8 Other specified diseases of liver
0.000 0.991 0.009
D69 Purpura and other haemorrhagic conditions
0.000 0.991 0.009
E89.4 Postprocedural ovarian failure
0.008 0.992 0.000
E88.2 Lipomatosis, not elsewhere classified
0.008 0.992 0.000
E86 Volume depletion
0.008 0.992 0.000
D68.0 Von Willebrand's disease
0.000 0.992 0.008
U80.0 Penicillin resistant agent
0.000 0.992 0.008
M62.5 Muscle wasting and atrophy, not elsewhere classified
0.000 0.992 0.008
D69.5 Secondary thrombocytopenia
0.000 0.992 0.008
E88.8 Other specified metabolic disorders
0.007 0.992 0.000
M62.4 Contracture of muscle
0.000 0.992 0.007
M62.3 Immobility syndrome (paraplegic)
0.000 0.992 0.007
M62.2 Ischaemic infarction of muscle
0.000 0.992 0.007
D69.9 Haemorrhagic condition, unspecified
0.000 0.993 0.007
M62.9 Disorder of muscle, unspecified
0.000 0.993 0.007
D69.1 Qualitative platelet defects
0.000 0.993 0.007
M62.0 Diastasis of muscle
0.000 0.993 0.007
E88.9 Metabolic disorder, unspecified
0.007 0.993 0.000
K82.4 Cholesterolosis of gallbladder
0.000 0.993 0.007
M62.1 Other rupture of muscle (nontraumatic)
0.000 0.993 0.007
E88.1 Lipodystrophy, not elsewhere classified
0.007 0.993 0.000
M62.59 Muscle wasting and atrophy, not elsewhere classified (Site unspecified)
0.000 0.993 0.007
D69.2 Other nonthrombocytopenic purpura
0.000 0.993 0.007
M62.6 Muscle strain
0.000 0.993 0.006
E88.3 Tumour lysis syndrome
0.006 0.994 0.000
M62.56 Muscle wasting and atrophy, not elsewhere classified (Lower leg)
0.000 0.994 0.006
M62.51 Muscle wasting and atrophy, not elsewhere classified (Shoulder region)
0.000 0.994 0.006
M62.55 Muscle wasting and atrophy, not elsewhere classified (Pelvic region and thigh)
0.000 0.994 0.006
D68.8 Other specified coagulation defects
0.000 0.994 0.006
E89.2 Postprocedural hypoparathyroidism
0.006 0.994 0.000
U00-U49 Provisional assignment of new diseases of uncertain etiology or emergency use
0.000 0.994 0.006
M62.58 Muscle wasting and atrophy, not elsewhere classified (Other)
0.000 0.994 0.006
M62.57 Muscle wasting and atrophy, not elsewhere classified (Ankle and foot)
0.000 0.994 0.006
M62.53 Muscle wasting and atrophy, not elsewhere classified (Forearm)
0.000 0.994 0.006
M62.52 Muscle wasting and atrophy, not elsewhere classified (Upper arm)
0.000 0.994 0.006
D69.8 Other specified haemorrhagic conditions
0.000 0.994 0.006
D69.4 Other primary thrombocytopenia
0.000 0.994 0.006
E88.0 Disorders of plasma-protein metabolism, not elsewhere classified
0.006 0.994 0.000
M62.54 Muscle wasting and atrophy, not elsewhere classified (Hand)
0.000 0.994 0.006
M62.99 Disorder of muscle, unspecified (Site unspecified)
0.000 0.994 0.006
M62.29 Ischaemic infarction of muscle (Site unspecified)
0.000 0.994 0.005
M62.28 Ischaemic infarction of muscle (Other)
0.000 0.994 0.005
M62.27 Ischaemic infarction of muscle (Ankle and foot)
0.000 0.994 0.005
M62.26 Ischaemic infarction of muscle (Lower leg)
0.000 0.994 0.005
M62.25 Ischaemic infarction of muscle (Pelvic region and thigh)
0.000 0.994 0.005
M62.24 Ischaemic infarction of muscle (Hand)
0.000 0.994 0.005
M62.23 Ischaemic infarction of muscle (Forearm)
0.000 0.994 0.005
M62.22 Ischaemic infarction of muscle (Upper arm)
0.000 0.994 0.005
M62.21 Ischaemic infarction of muscle (Shoulder region)
0.000 0.994 0.005
M62.20 Ischaemic infarction of muscle (Multiple sites)
0.000 0.994 0.005
M62.39 Immobility syndrome (paraplegic) (Site unspecified)
0.000 0.994 0.005
M62.38 Immobility syndrome (paraplegic) (Other)
0.000 0.994 0.005
M62.37 Immobility syndrome (paraplegic) (Ankle and foot)
0.000 0.994 0.005
M62.36 Immobility syndrome (paraplegic) (Lower leg)
0.000 0.994 0.005
M62.35 Immobility syndrome (paraplegic) (Pelvic region and thigh)
0.000 0.994 0.005
M62.34 Immobility syndrome (paraplegic) (Hand)
0.000 0.994 0.005
M62.33 Immobility syndrome (paraplegic) (Forearm)
0.000 0.994 0.005
M62.32 Immobility syndrome (paraplegic) (Upper arm)
0.000 0.994 0.005
M62.31 Immobility syndrome (paraplegic) (Shoulder region)
0.000 0.994 0.005
M62.30 Immobility syndrome (paraplegic) (Multiple sites)
0.000 0.994 0.005
M62.49 Contracture of muscle (Site unspecified)
0.000 0.994 0.005
M62.48 Contracture of muscle (Other)
0.000 0.994 0.005
M62.47 Contracture of muscle (Ankle and foot)
0.000 0.994 0.005
M62.46 Contracture of muscle (Lower leg)
0.000 0.994 0.005
M62.45 Contracture of muscle (Pelvic region and thigh)
0.000 0.994 0.005
M62.44 Contracture of muscle (Hand)
0.000 0.994 0.005
M62.43 Contracture of muscle (Forearm)
0.000 0.994 0.005
M62.42 Contracture of muscle (Upper arm)
0.000 0.994 0.005
M62.41 Contracture of muscle (Shoulder region)
0.000 0.994 0.005
M62.40 Contracture of muscle (Multiple sites)
0.000 0.994 0.005
M62.98 Disorder of muscle, unspecified (Other)
0.000 0.994 0.005
M62.97 Disorder of muscle, unspecified (Ankle and foot)
0.000 0.994 0.005
M62.95 Disorder of muscle, unspecified (Pelvic region and thigh)
0.000 0.994 0.005
M62.94 Disorder of muscle, unspecified (Hand)
0.000 0.994 0.005
M62.93 Disorder of muscle, unspecified (Forearm)
0.000 0.994 0.005
M62.92 Disorder of muscle, unspecified (Upper arm)
0.000 0.994 0.005
M62.91 Disorder of muscle, unspecified (Shoulder region)
0.000 0.994 0.005
M62.90 Disorder of muscle, unspecified (Multiple sites)
0.000 0.994 0.005
D69.0 Allergic purpura
0.000 0.994 0.005
M62.65 Muscle strain (Pelvic region and thigh)
0.000 0.995 0.005
N30.0 Acute cystitis
0.005 0.995 0.000
M62.09 Diastasis of muscle (Site unspecified)
0.000 0.995 0.005
M62.07 Diastasis of muscle (Ankle and foot)
0.000 0.995 0.005
M62.06 Diastasis of muscle (Lower leg)
0.000 0.995 0.005
M62.05 Diastasis of muscle (Pelvic region and thigh)
0.000 0.995 0.005
M62.04 Diastasis of muscle (Hand)
0.000 0.995 0.005
M62.03 Diastasis of muscle (Forearm)
0.000 0.995 0.005
M62.02 Diastasis of muscle (Upper arm)
0.000 0.995 0.005
M62.01 Diastasis of muscle (Shoulder region)
0.000 0.995 0.005
M62.00 Diastasis of muscle (Multiple sites)
0.000 0.995 0.005
M62.15 Other rupture of muscle (nontraumatic) (Pelvic region and thigh)
0.000 0.995 0.005
M62.96 Disorder of muscle, unspecified (Lower leg)
0.000 0.995 0.005
U51 Admission status on psychiatric patients
0.000 0.995 0.005
M62.19 Other rupture of muscle (nontraumatic) (Site unspecified)
0.000 0.995 0.005
M62.18 Other rupture of muscle (nontraumatic) (Other)
0.000 0.995 0.005
M62.17 Other rupture of muscle (nontraumatic) (Ankle and foot)
0.000 0.995 0.005
M62.16 Other rupture of muscle (nontraumatic) (Lower leg)
0.000 0.995 0.005
M62.14 Other rupture of muscle (nontraumatic) (Hand)
0.000 0.995 0.005
M62.13 Other rupture of muscle (nontraumatic) (Forearm)
0.000 0.995 0.005
M62.12 Other rupture of muscle (nontraumatic) (Upper arm)
0.000 0.995 0.005
M62.10 Other rupture of muscle (nontraumatic) (Multiple sites)
0.000 0.995 0.005
M62.50 Muscle wasting and atrophy, not elsewhere classified (Multiple sites)
0.000 0.995 0.005
M62.69 Muscle strain (Site unspecified)
0.000 0.995 0.005
M62.67 Muscle strain (Ankle and foot)
0.000 0.995 0.005
M62.64 Muscle strain (Hand)
0.000 0.995 0.005
M62.63 Muscle strain (Forearm)
0.000 0.995 0.005
M62.62 Muscle strain (Upper arm)
0.000 0.995 0.005
M62.61 Muscle strain (Shoulder region)
0.000 0.995 0.005
M62.60 Muscle strain (Multiple sites)
0.000 0.995 0.005
U51.1 Previously admitted to a psychiatric hospital of the provider
0.000 0.995 0.005
M62.08 Diastasis of muscle (Other)
0.000 0.995 0.005
C44.4 Skin of scalp and neck
0.005 0.995 0.000
D37.4 Colon
0.005 0.995 0.000
D68.2 Hereditary deficiency of other clotting factors
0.000 0.995 0.005
I25.9 Chronic ischaemic heart disease, unspecified
0.000 0.995 0.005
N75 Diseases of Bartholin's gland
0.000 0.995 0.005
U50 Level of care administered to neonates
0.000 0.995 0.004
U07 Emergency use of U07
0.000 0.995 0.004
U06 Emergency use of U06
0.000 0.995 0.004
U04 Severe acute respiratory syndrome [SARS]
0.000 0.995 0.004
U52 First in a series of a regular day/night admissions
0.000 0.995 0.004
M62.11 Other rupture of muscle (nontraumatic) (Shoulder region)
0.000 0.995 0.004
M62.68 Muscle strain (Other)
0.000 0.996 0.004
D72.8 Other specified disorders of white blood cells
0.000 0.996 0.004
M34.1 CR(E)ST syndrome
0.000 0.996 0.004
U51.2 Previously admitted to a psychiatric hospital of another provider
0.000 0.996 0.004
Z96.8 Presence of other specified functional implants
0.000 0.996 0.004
M62.66 Muscle strain (Lower leg)
0.000 0.996 0.004
M47.26 Other spondylosis with radiculopathy (Lumbar region)
0.000 0.996 0.004
K41.9 Unilateral or unspecified femoral hernia, without obstruction or gangrene
0.000 0.996 0.004
U81 Agent resistant to vancomycin and related antibiotics
0.000 0.996 0.004
Z93.6 Other artificial openings of urinary tract status
0.000 0.996 0.004
K46.9 Unspecified abdominal hernia without obstruction or gangrene
0.004 0.996 0.000
M60-M63 Disorders of muscles
0.000 0.996 0.004
N75.8 Other diseases of Bartholin's gland
0.000 0.996 0.004
U04.9 Severe acute respiratory syndrome [SARS], unspecified
0.000 0.996 0.003
U06.9 Emergency use of U06.9
0.000 0.996 0.003
U06.8 Emergency use of U06.8
0.000 0.996 0.003
U06.7 Emergency use of U06.7
0.000 0.996 0.003
U06.6 Emergency use of U06.6
0.000 0.996 0.003
U06.5 Emergency use of U06.5
0.000 0.996 0.003
U06.4 Emergency use of U06.4
0.000 0.996 0.003
U06.3 Emergency use of U06.3
0.000 0.996 0.003
U06.2 Emergency use of U06.2
0.000 0.996 0.003
U06.1 Emergency use of U06.1
0.000 0.996 0.003
U06.0 Emergency use of U06.0
0.000 0.996 0.003
U07.9 Emergency use of U07.9
0.000 0.996 0.003
U07.8 Emergency use of U07.8
0.000 0.996 0.003
U07.7 Emergency use of U07.7
0.000 0.996 0.003
U07.6 Emergency use of U07.6
0.000 0.996 0.003
U07.5 Emergency use of U07.5
0.000 0.996 0.003
U07.4 Emergency use of U07.4
0.000 0.996 0.003
U07.3 Emergency use of U07.3
0.000 0.996 0.003
U07.2 Emergency use of U07.2
0.000 0.996 0.003
U07.1 Emergency use of U07.1
0.000 0.996 0.003
U07.0 Emergency use of U07.0
0.000 0.996 0.003
U50.9 Inquest Adjourned Death
0.000 0.996 0.003
U50.3 Level of care administered to neonates (Maximal Intensive Care)
0.000 0.996 0.003
U50.2 Level of care administered to neonates (High Dependancy Intensive Care)
0.000 0.996 0.003
U50.1 Level of care administered to neonates (Special Care)
0.000 0.996 0.003
U50.0 Level of care administered to neonates (Normal Care)
0.000 0.996 0.003
M17.3 Other posttraumatic gonarthrosis
0.000 0.996 0.004
U51.0 Not Previously admitted to a psyciatric hospital
0.000 0.997 0.003
N75.9 Disease of Bartholin's gland, unspecified
0.000 0.997 0.003
I84.0 Internal thrombosed haemorrhoids
0.000 0.997 0.003
N75.1 Abscess of Bartholin's gland
0.000 0.997 0.003
Q82.8 Other specified congenital malformations of skin
0.003 0.997 0.000
Q82.0 Hereditary lymphoedema
0.003 0.997 0.000
Q82 Other congenital malformations of skin
0.003 0.997 0.000
Q82.2 Mastocytosis
0.003 0.997 0.000
I25.0 Atherosclerotic cardiovascular disease, so described
0.000 0.997 0.003
S46.2 Injury of muscle and tendon of other parts of biceps
0.000 0.997 0.003
Z80.1 Family history of malignant neoplasm of trachea, bronchus and lung
0.003 0.997 0.000
M63 Disorders of muscle in diseases classified elsewhere
0.000 0.997 0.003
M61 Calcification and ossification of muscle
0.000 0.997 0.003
D68.9 Coagulation defect, unspecified
0.000 0.997 0.003
R58 Haemorrhage, not elsewhere classified
0.003 0.997 0.000
U81.8 Agent resistant to other vancomycin-related antibiotic
0.000 0.997 0.003

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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