TreeWAS
Search
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
About
Frequently Asked Questions
Citation
Download association data
for this variant in csv format
Share this page

Variant-specific associations

rs3905495
log Bayes Factor = 60.1645
Chromosome 6   position 31,265,539  (GRCh37) Explore rs3905495 on Ensembl!

Hospitalization Episode Statistics (HES)

Self-Reported Statistics (SRS)

Hierarchical visualisation How to interpret this figure?
Associations at terminal nodes are shown if p(effect) ≥
Showing all nodes without filtering.
Click on a node to zoom (except terminal nodes).
Download this figure in format
Results table
Term Risk
posterior probability
 No effect
posterior probability
 Protective
posterior probability
  
E03.9 Hypothyroidism, unspecified
0.000 0.000 1.000
K90.0 Coeliac disease
0.000 0.000 1.000
L40.9 Psoriasis, unspecified
0.000 0.000 1.000
L40.5 Arthropathic psoriasis
0.000 0.000 1.000
L40 Psoriasis
0.000 0.000 1.000
M45.X9 Ankylosing spondylitis (Site unspecified)
0.000 0.002 0.998
M45 Ankylosing spondylitis
0.000 0.019 0.981
L40.0 Psoriasis vulgaris
0.000 0.024 0.976
M45.X0 Ankylosing spondylitis (Multiple sites in spine)
0.000 0.033 0.967
M07.39 Other psoriatic arthropathies (Site unspecified)
0.000 0.041 0.959
M07.3 Other psoriatic arthropathies
0.000 0.050 0.950
M07.30 Other psoriatic arthropathies (Multiple sites)
0.000 0.059 0.941
M45.X2 Ankylosing spondylitis (Cervical region)
0.000 0.097 0.903
M07.34 Other psoriatic arthropathies (Hand)
0.000 0.202 0.798
D50 Iron deficiency anaemia
0.000 0.226 0.774
D50.9 Iron deficiency anaemia, unspecified
0.000 0.226 0.774
D50-D53 Nutritional anaemias
0.000 0.229 0.771
D64.9 Anaemia, unspecified
0.000 0.231 0.769
D64 Other anaemias
0.000 0.231 0.769
D60-D64 Aplastic and other anaemias
0.000 0.231 0.769
M07.37 Other psoriatic arthropathies (Ankle and foot)
0.000 0.232 0.768
Chapter III Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
0.000 0.240 0.760
D61 Other aplastic anaemias
0.000 0.245 0.755
L40.3 Pustulosis palmaris et plantaris
0.000 0.247 0.753
D61.9 Aplastic anaemia, unspecified
0.000 0.252 0.748
L40.8 Other psoriasis
0.000 0.270 0.730
G35 Multiple sclerosis
0.000 0.272 0.728
L40.4 Guttate psoriasis
0.000 0.283 0.717
L40.2 Acrodermatitis continua
0.000 0.283 0.717
L40.1 Generalised pustular psoriasis
0.000 0.283 0.717
M45.X8 Ankylosing spondylitis (Sacral and sacrococcygeal region)
0.000 0.297 0.703
M45.X7 Ankylosing spondylitis (Lumbosacral region)
0.000 0.297 0.703
M45.X6 Ankylosing spondylitis (Lumbar region)
0.000 0.297 0.703
M45.X5 Ankylosing spondylitis (Thoracolumbar region)
0.000 0.297 0.703
M45.X4 Ankylosing spondylitis (Thoracic region)
0.000 0.297 0.703
M45.X3 Ankylosing spondylitis (Cervicothoracic region)
0.000 0.297 0.703
M45.X1 Ankylosing spondylitis (Occipito-atlanto-axial region)
0.000 0.297 0.703
R31 Unspecified haematuria
0.692 0.308 0.000
D50.8 Other iron deficiency anaemias
0.000 0.315 0.685
M07.36 Other psoriatic arthropathies (Lower leg)
0.000 0.318 0.681
M07.38 Other psoriatic arthropathies (Other)
0.000 0.319 0.681
M07.35 Other psoriatic arthropathies (Pelvic region and thigh)
0.000 0.319 0.681
M07.33 Other psoriatic arthropathies (Forearm)
0.000 0.319 0.681
M07.32 Other psoriatic arthropathies (Upper arm)
0.000 0.319 0.681
M07.31 Other psoriatic arthropathies (Shoulder region)
0.000 0.319 0.681
D80-D89 Certain disorders involving the immune mechanism
0.000 0.324 0.676
D51 Vitamin B12 deficiency anaemia
0.000 0.342 0.658
D52 Folate deficiency anaemia
0.000 0.358 0.642
D64.8 Other specified anaemias
0.000 0.373 0.627
E03 Other hypothyroidism
0.000 0.380 0.619
D89 Other disorders involving the immune mechanism, not elsewhere classified
0.000 0.419 0.580
D55-D59 Haemolytic anaemias
0.000 0.424 0.575
D51.0 Vitamin B12 deficiency anaemia due to intrinsic factor deficiency
0.000 0.428 0.572
D80 Immunodeficiency with predominantly antibody defects
0.000 0.432 0.568
D53 Other nutritional anaemias
0.000 0.433 0.567
D50.1 Sideropenic dysphagia
0.000 0.445 0.555
D64.4 Congenital dyserythropoietic anaemia
0.000 0.448 0.552
D64.3 Other sideroblastic anaemias
0.000 0.448 0.552
D64.2 Secondary sideroblastic anaemia due to drugs and toxins
0.000 0.448 0.552
D64.1 Secondary sideroblastic anaemia due to disease
0.000 0.448 0.552
D64.0 Hereditary sideroblastic anaemia
0.000 0.448 0.552
D51.9 Vitamin B12 deficiency anaemia, unspecified
0.000 0.451 0.549
D52.9 Folate deficiency anaemia, unspecified
0.000 0.451 0.549
D60 Acquired pure red cell aplasia [erythroblastopenia]
0.000 0.452 0.548
D50.0 Iron deficiency anaemia secondary to blood loss (chronic)
0.000 0.458 0.542
D61.8 Other specified aplastic anaemias
0.000 0.459 0.541
D61.3 Idiopathic aplastic anaemia
0.000 0.459 0.541
D61.2 Aplastic anaemia due to other external agents
0.000 0.459 0.541
E03.8 Other specified hypothyroidism
0.000 0.464 0.536
D61.0 Constitutional aplastic anaemia
0.000 0.488 0.512
D86 Sarcoidosis
0.000 0.493 0.507
D61.1 Drug-induced aplastic anaemia
0.000 0.497 0.503
D83 Common variable immunodeficiency
0.000 0.500 0.500
D81 Combined immunodeficiencies
0.000 0.515 0.484
D59 Acquired haemolytic anaemia
0.000 0.516 0.484
E03.2 Hypothyroidism due to medicaments and other exogenous substances
0.000 0.520 0.480
D84 Other immunodeficiencies
0.000 0.521 0.479
D51.2 Transcobalamin II deficiency
0.000 0.528 0.472
D51.1 Vitamin B12 deficiency anaemia due to selective vitamin B12 malabsorption with proteinuria
0.000 0.528 0.472
D89.0 Polyclonal hypergammaglobulinaemia
0.000 0.531 0.469
D89.9 Disorder involving the immune mechanism, unspecified
0.000 0.533 0.467
D52.8 Other folate deficiency anaemias
0.000 0.540 0.460
D52.1 Drug-induced folate deficiency anaemia
0.000 0.540 0.460
D52.0 Dietary folate deficiency anaemia
0.000 0.540 0.460
D80.2 Selective deficiency of immunoglobulin A [IgA]
0.000 0.542 0.457
D80.1 Nonfamilial hypogammaglobulinaemia
0.000 0.544 0.456
E03.5 Myxoedema coma
0.000 0.556 0.444
E03.4 Atrophy of thyroid (acquired)
0.000 0.556 0.444
E03.3 Postinfectious hypothyroidism
0.000 0.556 0.444
D86.3 Sarcoidosis of skin
0.000 0.558 0.442
D51.8 Other vitamin B12 deficiency anaemias
0.000 0.563 0.437
D86.0 Sarcoidosis of lung
0.000 0.564 0.436
D58 Other hereditary haemolytic anaemias
0.000 0.568 0.432
D89.1 Cryoglobulinaemia
0.000 0.570 0.430
D89.2 Hypergammaglobulinaemia, unspecified
0.000 0.579 0.421
D53.9 Nutritional anaemia, unspecified
0.000 0.579 0.421
D82 Immunodeficiency associated with other major defects
0.000 0.582 0.418
E03.0 Congenital hypothyroidism with diffuse goitre
0.000 0.582 0.417
D89.8 Other specified disorders involving the immune mechanism, not elsewhere classified
0.000 0.584 0.416
D89.3 Immune reconstitution syndrome
0.000 0.584 0.416
D80.9 Immunodeficiency with predominantly antibody defects, unspecified
0.000 0.585 0.415
D55 Anaemia due to enzyme disorders
0.000 0.587 0.413
D62 Acute posthaemorrhagic anaemia
0.000 0.590 0.410
D59.1 Other autoimmune haemolytic anaemias
0.000 0.590 0.410
D51.3 Other dietary vitamin B12 deficiency anaemia
0.000 0.592 0.408
D80.8 Other immunodeficiencies with predominantly antibody defects
0.000 0.592 0.407
D80.7 Transient hypogammaglobulinaemia of infancy
0.000 0.592 0.407
D80.6 Antibody deficiency with near-normal immunoglobulins or with hyperimmunoglobulinaemia
0.000 0.592 0.407
D80.5 Immunodeficiency with increased immunoglobulin M [IgM]
0.000 0.592 0.407
D80.0 Hereditary hypogammaglobulinaemia
0.000 0.592 0.407
D53.8 Other specified nutritional anaemias
0.000 0.593 0.407
D53.2 Scorbutic anaemia
0.000 0.593 0.407
D53.1 Other megaloblastic anaemias, not elsewhere classified
0.000 0.593 0.407
D53.0 Protein deficiency anaemia
0.000 0.593 0.407
E03.1 Congenital hypothyroidism without goitre
0.000 0.593 0.407
D80.3 Selective deficiency of immunoglobulin G [IgG] subclasses
0.000 0.594 0.406
M07 Psoriatic and enteropathic arthropathies
0.000 0.599 0.401
D80.4 Selective deficiency of immunoglobulin M [IgM]
0.000 0.599 0.401
D57 Sickle-cell disorders
0.000 0.607 0.393
D60.8 Other acquired pure red cell aplasias
0.000 0.607 0.393
D60.1 Transient acquired pure red cell aplasia
0.000 0.607 0.393
D60.0 Chronic acquired pure red cell aplasia
0.000 0.607 0.393
D60.9 Acquired pure red cell aplasia, unspecified
0.000 0.610 0.389
D84.9 Immunodeficiency, unspecified
0.000 0.617 0.383
D83.9 Common variable immunodeficiency, unspecified
0.000 0.626 0.373
D86.1 Sarcoidosis of lymph nodes
0.000 0.634 0.366
D59.9 Acquired haemolytic anaemia, unspecified
0.000 0.637 0.363
D83.8 Other common variable immunodeficiencies
0.000 0.642 0.358
D83.2 Common variable immunodeficiency with autoantibodies to B- or T-cells
0.000 0.642 0.358
D83.1 Common variable immunodeficiency with predominant immunoregulatory T-cell disorders
0.000 0.642 0.358
D83.0 Common variable immunodeficiency with predominant abnormalities of B-cell numbers and function
0.000 0.642 0.358
D81.9 Combined immunodeficiency, unspecified
0.000 0.652 0.347
D81.8 Other combined immunodeficiencies
0.000 0.652 0.347
D81.7 Major histocompatibility complex class II deficiency
0.000 0.652 0.347
D81.6 Major histocompatibility complex class I deficiency
0.000 0.652 0.347
D81.5 Purine nucleoside phosphorylase [PNP] deficiency
0.000 0.652 0.347
D81.4 Nezelof's syndrome
0.000 0.652 0.347
D81.3 Adenosine deaminase [ADA] deficiency
0.000 0.652 0.347
D81.2 Severe combined immunodeficiency [SCID] with low or normal B-cell numbers
0.000 0.652 0.347
D81.1 Severe combined immunodeficiency [SCID] with low T- and B-cell numbers
0.000 0.652 0.347
D81.0 Severe combined immunodeficiency [SCID] with reticular dysgenesis
0.000 0.652 0.347
D84.1 Defects in the complement system
0.000 0.652 0.347
D59.8 Other acquired haemolytic anaemias
0.000 0.653 0.347
D59.6 Haemoglobinuria due to haemolysis from other external causes
0.000 0.653 0.347
D59.5 Paroxysmal nocturnal haemoglobinuria [Marchiafava-Micheli]
0.000 0.653 0.347
D59.4 Other nonautoimmune haemolytic anaemias
0.000 0.653 0.347
D59.3 Haemolytic-uraemic syndrome
0.000 0.653 0.347
D59.2 Drug-induced nonautoimmune haemolytic anaemia
0.000 0.653 0.347
D59.0 Drug-induced autoimmune haemolytic anaemia
0.000 0.653 0.347
D86.2 Sarcoidosis of lung with sarcoidosis of lymph nodes
0.000 0.656 0.344
D84.0 Lymphocyte function antigen-1 [LFA-1] defect
0.000 0.656 0.343
D58.0 Hereditary spherocytosis
0.000 0.663 0.337
D56 Thalassaemia
0.000 0.663 0.337
D58.9 Hereditary haemolytic anaemia, unspecified
0.000 0.668 0.332
D86.9 Sarcoidosis, unspecified
0.000 0.677 0.323
D58.8 Other specified hereditary haemolytic anaemias
0.000 0.690 0.310
D58.1 Hereditary elliptocytosis
0.000 0.690 0.310
D82.9 Immunodeficiency associated with major defect, unspecified
0.000 0.700 0.300
D82.8 Immunodeficiency associated with other specified major defects
0.000 0.700 0.300
D82.4 Hyperimmunoglobulin E [IgE] syndrome
0.000 0.700 0.300
D82.3 Immunodeficiency following hereditary defective response to Epstein-Barr virus
0.000 0.700 0.300
D82.2 Immunodeficiency with short-limbed stature
0.000 0.700 0.300
D82.0 Wiskott-Aldrich syndrome
0.000 0.700 0.300
D55.9 Anaemia due to enzyme disorder, unspecified
0.000 0.704 0.296
D55.8 Other anaemias due to enzyme disorders
0.000 0.704 0.296
D55.3 Anaemia due to disorders of nucleotide metabolism
0.000 0.704 0.296
D55.2 Anaemia due to disorders of glycolytic enzymes
0.000 0.704 0.296
D55.1 Anaemia due to other disorders of glutathione metabolism
0.000 0.704 0.296
D55.0 Anaemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
0.000 0.704 0.296
M07.6 Other enteropathic arthropathies
0.000 0.712 0.288
M07.5 Arthropathy in ulcerative colitis
0.000 0.712 0.288
M07.4 Arthropathy in Crohn's disease [regional enteritis]
0.000 0.712 0.288
M07.2 Psoriatic spondylitis
0.000 0.712 0.288
M07.1 Arthritis mutilans
0.000 0.712 0.288
M07.0 Distal interphalangeal psoriatic arthropathy
0.000 0.712 0.288
D63 Anaemia in chronic diseases classified elsewhere
0.000 0.712 0.287
D57.8 Other sickle-cell disorders
0.000 0.718 0.282
D57.3 Sickle-cell trait
0.000 0.718 0.282
D57.2 Double heterozygous sickling disorders
0.000 0.718 0.282
D57.0 Sickle-cell anaemia with crisis
0.000 0.718 0.282
D84.8 Other specified immunodeficiencies
0.000 0.726 0.274
D58.2 Other haemoglobinopathies
0.000 0.729 0.271
D57.1 Sickle-cell anaemia without crisis
0.000 0.737 0.262
D56.9 Thalassaemia, unspecified
0.000 0.758 0.241
D56.8 Other thalassaemias
0.000 0.758 0.241
D56.4 Hereditary persistence of foetal haemoglobin [HPFH]
0.000 0.758 0.241
D56.2 Delta-beta thalassaemia
0.000 0.758 0.241
D56.0 Alpha thalassaemia
0.000 0.758 0.241
D56.1 Beta thalassaemia
0.000 0.760 0.240
L40-L45 Papulosquamous disorders
0.000 0.761 0.239
D82.1 Di George's syndrome
0.001 0.767 0.233
K90 Intestinal malabsorption
0.000 0.777 0.223
M07.09 Distal interphalangeal psoriatic arthropathy (Site unspecified)
0.000 0.793 0.206
M07.08 Distal interphalangeal proriatic arthropathy-Other
0.000 0.793 0.206
M07.07 Distal interphalangeal psoriatic arthropathy (Ankle and foot)
0.000 0.793 0.206
M07.06 Distal interphalangeal proriatic arthropathy-Lower leg
0.000 0.793 0.206
M07.05 Distal interphalangeal proriatic arthropathy-Pelvic/thigh
0.000 0.793 0.206
M07.04 Distal interphalangeal psoriatic arthropathy (Hand)
0.000 0.793 0.206
M07.03 Distal interphalangeal proriatic arthropathy-Forearm
0.000 0.793 0.206
M07.02 Distal interphalangeal proriatic arthropathy-Upper arm
0.000 0.793 0.206
M07.01 Distal interphalangeal proriatic arthropathy-Shldr region
0.000 0.793 0.206
M07.00 Distal interphalangeal psoriatic arthropathy (Multiple sites)
0.000 0.793 0.206
M07.19 Arthritis mutilans (Site unspecified)
0.000 0.793 0.206
M07.18 Arthritis mutilans (Other)
0.000 0.793 0.206
M07.17 Arthritis mutilans (Ankle and foot)
0.000 0.793 0.206
M07.16 Arthritis mutilans (Lower leg)
0.000 0.793 0.206
M07.15 Arthritis mutilans (Pelvic region and thigh)
0.000 0.793 0.206
M07.14 Arthritis mutilans (Hand)
0.000 0.793 0.206
M07.13 Arthritis mutilans (Forearm)
0.000 0.793 0.206
M07.12 Arthritis mutilans (Upper arm)
0.000 0.793 0.206
M07.11 Arthritis mutilans (Shoulder region)
0.000 0.793 0.206
M07.10 Arthritis mutilans (Multiple sites)
0.000 0.793 0.206
M07.29 Psoriatic spondylitis (Site unspecified)
0.000 0.793 0.206
M07.28 Psoriatic spondylitis (Other)
0.000 0.793 0.206
M07.27 Psoriatic spondylitis (Ankle and foot)
0.000 0.793 0.206
M07.26 Psoriatic spondylitis (Lower leg)
0.000 0.793 0.206
M07.25 Psoriatic spondylitis (Pelvic region and thigh)
0.000 0.793 0.206
M07.24 Psoriatic spondylitis (Hand)
0.000 0.793 0.206
M07.23 Psoriatic spondylitis (Forearm)
0.000 0.793 0.206
M07.22 Psoriatic spondylitis (Upper arm)
0.000 0.793 0.206
M07.21 Psoriatic spondylitis (Shoulder region)
0.000 0.793 0.206
M07.20 Psoriatic spondylitis (Multiple sites)
0.000 0.793 0.206
M07.49 Arthropathy in Crohn's disease [regional enteritis] (Site unspecified)
0.000 0.793 0.206
M07.48 Arthropathy in Crohn's disease [regional enteritis] (Other)
0.000 0.793 0.206
M07.47 Arthropathy in Crohn's disease [regional enteritis] (Ankle and foot)
0.000 0.793 0.206
M07.46 Arthropathy in Crohn's disease [regional enteritis] (Lower leg)
0.000 0.793 0.206
M07.45 Arthropathy in Crohn's disease [regional enteritis] (Pelvic region and thigh)
0.000 0.793 0.206
M07.44 Arthropathy in Crohn's disease [regional enteritis] (Hand)
0.000 0.793 0.206
M07.43 Arthropathy in Crohn's disease [regional enteritis] (Forearm)
0.000 0.793 0.206
M07.42 Arthropathy in Crohn's disease [regional enteritis] (Upper arm)
0.000 0.793 0.206
M07.41 Arthropathy in Crohn's disease [regional enteritis] (Shoulder region)
0.000 0.793 0.206
M07.40 Arthropathy in Crohn's disease [regional enteritis] (Multiple sites)
0.000 0.793 0.206
M07.59 Arthropathy in ulcerative colitis (Site unspecified)
0.000 0.793 0.206
M07.58 Arthropathy in ulcerative colitis (Other)
0.000 0.793 0.206
M07.57 Arthropathy in ulcerative colitis (Ankle and foot)
0.000 0.793 0.206
M07.56 Arthropathy in ulcerative colitis (Lower leg)
0.000 0.793 0.206
M07.55 Arthropathy in ulcerative colitis (Pelvic region and thigh)
0.000 0.793 0.206
M07.54 Arthropathy in ulcerative colitis (Hand)
0.000 0.793 0.206
M07.53 Arthropathy in ulcerative colitis (Forearm)
0.000 0.793 0.206
M07.52 Arthropathy in ulcerative colitis (Upper arm)
0.000 0.793 0.206
M07.51 Arthropathy in ulcerative colitis (Shoulder region)
0.000 0.793 0.206
M07.50 Arthropathy in ulcerative colitis (Multiple sites)
0.000 0.793 0.206
M07.69 Other enteropathic arthropathies (Site unspecified)
0.000 0.793 0.206
M07.68 Other enteropathic arthropathies (Other)
0.000 0.793 0.206
M07.67 Other enteropathic arthropathies (Ankle and foot)
0.000 0.793 0.206
M07.66 Other enteropathic arthropathies (Lower leg)
0.000 0.793 0.206
M07.65 Other enteropathic arthropathies (Pelvic region and thigh)
0.000 0.793 0.206
M07.64 Other enteropathic arthropathies (Hand)
0.000 0.793 0.206
M07.63 Other enteropathic arthropathies (Forearm)
0.000 0.793 0.206
M07.62 Other enteropathic arthropathies (Upper arm)
0.000 0.793 0.206
M07.61 Other enteropathic arthropathies (Shoulder region)
0.000 0.793 0.206
M07.60 Other enteropathic arthropathies (Multiple sites)
0.000 0.793 0.206
D63.1 Anaemia in other chronic diseases classified elsewhere
0.000 0.794 0.206
D65-D69 Coagulation defects, purpura and other haemorrhagic conditions
0.000 0.802 0.198
D70-D77 Other diseases of blood and blood-forming organs
0.000 0.810 0.190
G35-G37 Demyelinating diseases of the central nervous system
0.000 0.825 0.175
L44 Other papulosquamous disorders
0.000 0.828 0.171
L41 Parapsoriasis
0.000 0.828 0.171
L45 Papulosquamous disorders in diseases classified elsewhere
0.000 0.828 0.171
D56.3 Thalassaemia trait
0.001 0.831 0.168
D63.8 Anaemia in other chronic diseases classified elsewhere
0.000 0.834 0.166
L42 Pityriasis rosea
0.000 0.837 0.163
D72 Other disorders of white blood cells
0.000 0.839 0.161
K90.3 Pancreatic steatorrhoea
0.000 0.840 0.160
K90.2 Blind loop syndrome, not elsewhere classified
0.000 0.840 0.160
K90.1 Tropical sprue
0.000 0.840 0.160
J47 Bronchiectasis
0.149 0.851 0.000
D67 Hereditary factor IX deficiency
0.000 0.858 0.141
D72.1 Eosinophilia
0.000 0.861 0.139
K90.4 Malabsorption due to intolerance, not elsewhere classified
0.000 0.862 0.138
D74 Methaemoglobinaemia
0.000 0.864 0.136
D77 Other disorders of blood and blood-forming organs in diseases classified elsewhere
0.000 0.864 0.136
D71 Functional disorders of polymorphonuclear neutrophils
0.000 0.864 0.136
K90.8 Other intestinal malabsorption
0.000 0.865 0.135
D76 Certain diseases involving lymphoreticular tissue and reticulohistiocytic system
0.000 0.866 0.134
D66 Hereditary factor VIII deficiency
0.000 0.869 0.131
K90.9 Intestinal malabsorption, unspecified
0.000 0.870 0.130
D86.8 Sarcoidosis of other and combined sites
0.002 0.872 0.126
D69 Purpura and other haemorrhagic conditions
0.000 0.873 0.127
L41.9 Parapsoriasis, unspecified
0.000 0.877 0.123
L41.8 Other parapsoriasis
0.000 0.877 0.123
L41.5 Retiform parapsoriasis
0.000 0.877 0.123
L41.4 Large plaque parapsoriasis
0.000 0.877 0.123
L41.3 Small plaque parapsoriasis
0.000 0.877 0.123
L41.2 Lymphomatoid papulosis
0.000 0.877 0.123
L41.1 Pityriasis lichenoides chronica
0.000 0.877 0.123
L41.0 Pityriasis lichenoides et varioliformis acuta
0.000 0.877 0.123
L44.9 Papulosquamous disorder, unspecified
0.000 0.877 0.123
L44.8 Other specified papulosquamous disorders
0.000 0.877 0.123
L44.4 Infantile papular acrodermatitis [Giannotti-Crosti]
0.000 0.877 0.123
L44.3 Lichen ruber moniliformis
0.000 0.877 0.123
L44.2 Lichen striatus
0.000 0.877 0.123
L44.1 Lichen nitidus
0.000 0.877 0.123
L44.0 Pityriasis rubra pilaris
0.000 0.877 0.123
D65 Disseminated intravascular coagulation [defibrination syndrome]
0.000 0.880 0.120
D72.8 Other specified disorders of white blood cells
0.000 0.880 0.120
G36 Other acute disseminated demyelination
0.000 0.883 0.117
D72.9 Disorder of white blood cells, unspecified
0.000 0.884 0.116
D72.0 Genetic anomalies of leukocytes
0.000 0.884 0.116
K75 Other inflammatory liver diseases
0.000 0.890 0.110
K75.8 Other specified inflammatory liver diseases
0.000 0.892 0.108
D69.4 Other primary thrombocytopenia
0.000 0.893 0.107
K75.4 Autoimmune hepatitis
0.000 0.893 0.107
E00-E07 Disorders of thyroid gland
0.000 0.894 0.106
K75.0 Abscess of liver
0.000 0.896 0.104
D69.6 Thrombocytopenia, unspecified
0.000 0.900 0.100
D69.2 Other nonthrombocytopenic purpura
0.000 0.900 0.100
D74.9 Methaemoglobinaemia, unspecified
0.000 0.902 0.098
D74.8 Other methaemoglobinaemias
0.000 0.902 0.098
D74.0 Congenital methaemoglobinaemia
0.000 0.902 0.098
E05 Thyrotoxicosis [hyperthyroidism]
0.000 0.903 0.097
D76.2 Haemophagocytic syndrome, infection-associated
0.000 0.904 0.096
D76.1 Haemophagocytic lymphohistiocytosis
0.000 0.904 0.096
D76.0 Langerhans' cell histiocytosis, not elsewhere classified
0.000 0.904 0.096
D69.5 Secondary thrombocytopenia
0.000 0.905 0.095
D76.3 Other histiocytosis syndromes
0.000 0.906 0.094
E05.0 Thyrotoxicosis with diffuse goitre
0.000 0.906 0.094
D73 Diseases of spleen
0.000 0.907 0.093
D69.8 Other specified haemorrhagic conditions
0.000 0.908 0.092
K70-K77 Diseases of liver
0.000 0.914 0.086
G36.9 Acute disseminated demyelination, unspecified
0.000 0.916 0.084
G36.8 Other specified acute disseminated demyelination
0.000 0.916 0.084
G36.1 Acute and subacute haemorrhagic leukoencephalitis [Hurst]
0.000 0.916 0.084
E05.9 Thyrotoxicosis, unspecified
0.000 0.918 0.082
K70 Alcoholic liver disease
0.000 0.919 0.081
K72 Hepatic failure, not elsewhere classified
0.000 0.919 0.081
D69.1 Qualitative platelet defects
0.000 0.921 0.079
K75.2 Nonspecific reactive hepatitis
0.000 0.921 0.079
K75.1 Phlebitis of portal vein
0.000 0.921 0.079
K75.3 Granulomatous hepatitis, not elsewhere classified
0.000 0.923 0.077
D69.9 Haemorrhagic condition, unspecified
0.000 0.923 0.077
K73 Chronic hepatitis, not elsewhere classified
0.000 0.924 0.076
E01 Iodine-deficiency-related thyroid disorders and allied conditions
0.000 0.924 0.076
E00 Congenital iodine-deficiency syndrome
0.000 0.924 0.076
K72.9 Hepatic failure, unspecified
0.000 0.924 0.076
G36.0 Neuromyelitis optica [Devic]
0.000 0.924 0.075
K70.4 Alcoholic hepatic failure
0.000 0.926 0.074
L43 Lichen planus
0.000 0.926 0.073
D69.0 Allergic purpura
0.000 0.927 0.072
K70.1 Alcoholic hepatitis
0.000 0.927 0.073
D73.5 Infarction of spleen
0.000 0.928 0.072
D69.3 Idiopathic thrombocytopenic purpura
0.000 0.930 0.070
E05.5 Thyroid crisis or storm
0.000 0.930 0.070
E05.4 Thyrotoxicosis factitia
0.000 0.930 0.070
E05.3 Thyrotoxicosis from ectopic thyroid tissue
0.000 0.930 0.070
E05.1 Thyrotoxicosis with toxic single thyroid nodule
0.000 0.930 0.070
D73.4 Cyst of spleen
0.000 0.931 0.069
D73.1 Hypersplenism
0.000 0.932 0.068
D73.2 Chronic congestive splenomegaly
0.000 0.933 0.067
K72.0 Acute and subacute hepatic failure
0.000 0.933 0.067
E02 Subclinical iodine-deficiency hypothyroidism
0.000 0.934 0.066
E78.0 Pure hypercholesterolaemia
0.066 0.934 0.000
K73.9 Chronic hepatitis, unspecified
0.000 0.935 0.065
K73.2 Chronic active hepatitis, not elsewhere classified
0.000 0.935 0.065
G37 Other demyelinating diseases of central nervous system
0.000 0.936 0.063
D73.9 Disease of spleen, unspecified
0.000 0.937 0.063
K77 Liver disorders in diseases classified elsewhere
0.000 0.938 0.062
D73.3 Abscess of spleen
0.000 0.939 0.061
K70.0 Alcoholic fatty liver
0.000 0.939 0.061
E07 Other disorders of thyroid
0.000 0.940 0.060
K70.2 Alcoholic fibrosis and sclerosis of liver
0.000 0.941 0.058
N39.3 Stress incontinence
0.058 0.942 0.000
D63.0 Anaemia in neoplastic disease
0.000 0.943 0.057
K71 Toxic liver disease
0.000 0.943 0.057
K70.9 Alcoholic liver disease, unspecified
0.000 0.945 0.055
K73.1 Chronic lobular hepatitis, not elsewhere classified
0.000 0.945 0.055
K73.0 Chronic persistent hepatitis, not elsewhere classified
0.000 0.945 0.055
E00.9 Congenital iodine-deficiency syndrome, unspecified
0.000 0.945 0.055
E00.2 Congenital iodine-deficiency syndrome, mixed type
0.000 0.945 0.055
E00.1 Congenital iodine-deficiency syndrome, myxoedematous type
0.000 0.945 0.055
E00.0 Congenital iodine-deficiency syndrome, neurological type
0.000 0.945 0.055
E01.8 Other iodine-deficiency-related thyroid disorders and allied conditions
0.000 0.945 0.055
E01.2 Iodine-deficiency-related (endemic) goitre, unspecified
0.000 0.945 0.055
E01.1 Iodine-deficiency-related multinodular (endemic) goitre
0.000 0.945 0.055
E01.0 Iodine-deficiency-related diffuse (endemic) goitre
0.000 0.945 0.055
D73.8 Other diseases of spleen
0.000 0.945 0.054
L43.3 Subacute (active) lichen planus
0.000 0.947 0.053
L43.2 Lichenoid drug reaction
0.000 0.947 0.053
L43.1 Bullous lichen planus
0.000 0.947 0.053
L43.0 Hypertrophic lichen planus
0.000 0.947 0.053
E05.2 Thyrotoxicosis with toxic multinodular goitre
0.000 0.948 0.052
K75.9 Inflammatory liver disease, unspecified
0.000 0.948 0.052
K72.1 Chronic hepatic failure
0.000 0.948 0.052
K73.8 Other chronic hepatitis, not elsewhere classified
0.000 0.950 0.050
K70.3 Alcoholic cirrhosis of liver
0.000 0.950 0.050
E07.8 Other specified disorders of thyroid
0.000 0.951 0.049
G37.8 Other specified demyelinating diseases of central nervous system
0.000 0.953 0.047
D73.0 Hyposplenism
0.000 0.954 0.046
E06 Thyroiditis
0.000 0.954 0.046
G37.5 Concentric sclerosis [Balo]
0.000 0.954 0.045
G37.4 Subacute necrotising myelitis
0.000 0.954 0.045
G37.2 Central pontine myelinolysis
0.000 0.954 0.045
G37.1 Central demyelination of corpus callosum
0.000 0.954 0.045
G37.0 Diffuse sclerosis
0.000 0.954 0.045
E05.8 Other thyrotoxicosis
0.000 0.955 0.045
D70 Agranulocytosis
0.000 0.955 0.045
K77.8 Liver disorders in other diseases classified elsewhere
0.000 0.955 0.045
K77.0 Liver disorders in infectious and parasitic diseases classified elsewhere
0.000 0.955 0.045
E07.1 Dyshormogenetic goitre
0.000 0.956 0.043
E07.0 Hypersecretion of calcitonin
0.000 0.956 0.043
Chapter XII Diseases of the skin and subcutaneous tissue
0.000 0.959 0.041
K71.1 Toxic liver disease with hepatic necrosis
0.000 0.959 0.041
K71.9 Toxic liver disease, unspecified
0.000 0.959 0.041
K71.8 Toxic liver disease with other disorders of liver
0.000 0.959 0.041
K71.7 Toxic liver disease with fibrosis and cirrhosis of liver
0.000 0.959 0.041
K71.5 Toxic liver disease with chronic active hepatitis
0.000 0.959 0.041
K71.4 Toxic liver disease with chronic lobular hepatitis
0.000 0.959 0.041
K71.3 Toxic liver disease with chronic persistent hepatitis
0.000 0.959 0.041
K71.2 Toxic liver disease with acute hepatitis
0.000 0.959 0.041
K71.0 Toxic liver disease with cholestasis
0.000 0.959 0.041
L50 Urticaria
0.000 0.960 0.040
L50-L54 Urticaria and erythema
0.000 0.960 0.040
D75 Other diseases of blood and blood-forming organs
0.000 0.961 0.038
L50.9 Urticaria, unspecified
0.000 0.962 0.038
K29.6 Other gastritis
0.038 0.962 0.000
L52 Erythema nodosum
0.000 0.964 0.036
L10-L14 Bullous disorders
0.000 0.964 0.036
K71.6 Toxic liver disease with hepatitis, not elsewhere classified
0.000 0.965 0.035
E06.3 Autoimmune thyroiditis
0.000 0.965 0.035
L50.0 Allergic urticaria
0.000 0.966 0.034
L43.8 Other lichen planus
0.001 0.966 0.033
E06.4 Drug-induced thyroiditis
0.000 0.967 0.033
E06.2 Chronic thyroiditis with transient thyrotoxicosis
0.000 0.967 0.033
E06.0 Acute thyroiditis
0.000 0.967 0.033
N39 Other disorders of urinary system
0.033 0.967 0.000
E06.5 Other chronic thyroiditis
0.000 0.967 0.033
L50.1 Idiopathic urticaria
0.000 0.968 0.032
L13 Other bullous disorders
0.000 0.968 0.032
K74 Fibrosis and cirrhosis of liver
0.000 0.968 0.032
N39.8 Other specified disorders of urinary system
0.031 0.969 0.000
M45-M49 Spondylopathies
0.000 0.970 0.030
L55-L59 Radiation-related disorders of the skin and subcutaneous tissue
0.000 0.970 0.030
N39.9 Disorder of urinary system, unspecified
0.030 0.970 0.000
L13.0 Dermatitis herpetiformis
0.000 0.970 0.030
L50.8 Other urticaria
0.000 0.970 0.029
D75.9 Disease of blood and blood-forming organs, unspecified
0.000 0.971 0.029
K74.0 Hepatic fibrosis
0.000 0.971 0.029
L50.6 Contact urticaria
0.000 0.971 0.029
L50.5 Cholinergic urticaria
0.000 0.971 0.029
L50.4 Vibratory urticaria
0.000 0.971 0.029
L50.3 Dermatographic urticaria
0.000 0.971 0.029
L50.2 Urticaria due to cold and heat
0.000 0.971 0.029
L54 Erythema in diseases classified elsewhere
0.000 0.971 0.029
D75.0 Familial erythrocytosis
0.000 0.971 0.028
N39.1 Persistent proteinuria, unspecified
0.029 0.971 0.000
G31 Other degenerative diseases of nervous system, not elsewhere classified
0.000 0.973 0.027
L11 Other acantholytic disorders
0.000 0.974 0.026
L12 Pemphigoid
0.000 0.974 0.026
G37.3 Acute transverse myelitis in demyelinating disease of central nervous system
0.001 0.974 0.025
L14 Bullous disorders in diseases classified elsewhere
0.000 0.974 0.026
L10 Pemphigus
0.000 0.974 0.026
G31.8 Other specified degenerative diseases of nervous system
0.000 0.974 0.026
G30-G32 Other degenerative diseases of the nervous system
0.000 0.974 0.026
L56 Other acute skin changes due to ultraviolet radiation
0.000 0.975 0.025
Chapter VI Diseases of the nervous system
0.000 0.975 0.025
R30-R39 Symptoms and signs involving the urinary system
0.024 0.976 0.000
N39.2 Orthostatic proteinuria, unspecified
0.024 0.976 0.000
G31.2 Degeneration of nervous system due to alcohol
0.000 0.976 0.023
L13.9 Bullous disorder, unspecified
0.000 0.977 0.023
L13.8 Other specified bullous disorders
0.000 0.977 0.023
L13.1 Subcorneal pustular dermatitis
0.000 0.977 0.023
G37.9 Demyelinating disease of central nervous system, unspecified
0.000 0.977 0.023
K74.4 Secondary biliary cirrhosis
0.000 0.977 0.023
K74.2 Hepatic fibrosis with hepatic sclerosis
0.000 0.977 0.023
G62.9 Polyneuropathy, unspecified
0.000 0.977 0.023
G62 Other polyneuropathies
0.000 0.977 0.023
G60-G64 Polyneuropathies and other disorders of the peripheral nervous system
0.000 0.977 0.023
G31.0 Circumscribed brain atrophy
0.000 0.977 0.023
R33 Retention of urine
0.023 0.977 0.000
E06.1 Subacute thyroiditis
0.001 0.978 0.022
E04 Other non-toxic goitre
0.000 0.978 0.022
L59 Other disorders of skin and subcutaneous tissue related to radiation
0.000 0.978 0.022
L58 Radiodermatitis
0.000 0.978 0.022
L55 Sunburn
0.000 0.978 0.022
G31.9 Degenerative disease of nervous system, unspecified
0.000 0.978 0.022
K90-K93 Other diseases of the digestive system
0.000 0.978 0.022
K74.1 Hepatic sclerosis
0.000 0.978 0.021
L56.8 Other specified acute skin changes due to ultraviolet radiation
0.000 0.979 0.021
L54.8 Erythema in other diseases classified elsewhere
0.000 0.979 0.021
L54.0 Erythema marginatum in acute rheumatic fever
0.000 0.979 0.021
L08.8 Other specified local infections of skin and subcutaneous tissue
0.000 0.979 0.021
G70-G73 Diseases of myoneural junction and muscle
0.000 0.979 0.021
E06.9 Thyroiditis, unspecified
0.001 0.980 0.020
L53 Other erythematous conditions
0.000 0.980 0.020
G31.1 Senile degeneration of brain, not elsewhere classified
0.000 0.980 0.020
L11.0 Acquired keratosis follicularis
0.000 0.980 0.019
L51 Erythema multiforme
0.000 0.981 0.019
G32 Other degenerative disorders of nervous system in diseases classified elsewhere
0.000 0.981 0.019
G62.1 Alcoholic polyneuropathy
0.000 0.981 0.019
L12.9 Pemphigoid, unspecified
0.000 0.981 0.019
L11.9 Acantholytic disorder, unspecified
0.000 0.981 0.019
L11.8 Other specified acantholytic disorders
0.000 0.981 0.019
L11.1 Transient acantholytic dermatosis [Grover]
0.000 0.981 0.019
L12.0 Bullous pemphigoid
0.000 0.981 0.019
M49 Spondylopathies in diseases classified elsewhere
0.000 0.981 0.019
L12.8 Other pemphigoid
0.000 0.981 0.019
L12.3 Acquired epidermolysis bullosa
0.000 0.981 0.019
L12.2 Chronic bullous disease of childhood
0.000 0.981 0.019
L10.8 Other pemphigus
0.000 0.981 0.019
L10.5 Drug-induced pemphigus
0.000 0.981 0.019

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.

This website was created, designed, and edited by ORCID iD iconPatrick K. Albers

The contents of TreeWAS.org are available under the Creative Commons Attribution 4.0 International License (CC BY 4.0) with attribution (citation) required.

TreeWAS Database © 2019 - 2026 About Frequently Asked Questions Citation Contact Terms & Conditions This website does not use cookies to collect any personal information about you.