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Variant-specific associations

rs2225614
log Bayes Factor = <0.0001
Chromosome 9   position 24,111,280  (GRCh37) Explore rs2225614 on Ensembl!
Variant rs2225614 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
 
B34.9 Viral infection, unspecified
0.000 0.982 0.018
T85.6 Mechanical complication of other specified internal prosthetic devices, implants and grafts
0.017 0.983 0.000
Z87.8 Personal history of other specified conditions
0.012 0.988 0.000
Q61.3 Polycystic kidney, unspecified
0.011 0.989 0.000
Q61 Cystic kidney disease
0.011 0.989 0.000
T81.3 Disruption of operation wound, not elsewhere classified
0.000 0.990 0.010
Q60-Q64 Congenital malformations of the urinary system
0.010 0.990 0.000
C55 Malignant neoplasm of uterus, part unspecified
0.000 0.990 0.010
Q61.9 Cystic kidney disease, unspecified
0.010 0.990 0.000
J98.1 Pulmonary collapse
0.000 0.990 0.010
I22.0 Subsequent myocardial infarction of anterior wall
0.009 0.991 0.000
I22 Subsequent myocardial infarction
0.009 0.991 0.000
Q60 Renal agenesis and other reduction defects of kidney
0.009 0.991 0.000
I73.0 Raynaud's syndrome
0.009 0.991 0.000
I22.8 Subsequent myocardial infarction of other sites
0.009 0.991 0.000
Q63 Other congenital malformations of kidney
0.009 0.991 0.000
I22.1 Subsequent myocardial infarction of inferior wall
0.009 0.991 0.000
C51-C58 Malignant neoplasms of female genital organs
0.000 0.991 0.009
C56 Malignant neoplasm of ovary
0.000 0.991 0.009
Q61.0 Congenital single renal cyst
0.008 0.991 0.000
Q61.2 Polycystic kidney, adult type
0.008 0.991 0.000
R23.3 Spontaneous ecchymoses
0.008 0.992 0.000
Q64 Other congenital malformations of urinary system
0.008 0.992 0.000
Q61.8 Other cystic kidney diseases
0.008 0.992 0.000
Q61.4 Renal dysplasia
0.008 0.992 0.000
Q61.1 Polycystic kidney, infantile type
0.008 0.992 0.000
Q62 Congenital obstructive defects of renal pelvis and congenital malformations of ureter
0.008 0.992 0.000
Q61.5 Medullary cystic kidney
0.008 0.992 0.000
I22.9 Subsequent myocardial infarction of unspecified site
0.008 0.992 0.000
Q60.0 Renal agenesis, unilateral
0.008 0.992 0.000
B34 Viral infection of unspecified site
0.000 0.992 0.008
C54 Malignant neoplasm of corpus uteri
0.000 0.992 0.008
S05.8 Other injuries of eye and orbit
0.008 0.992 0.000
R23.8 Other and unspecified skin changes
0.008 0.992 0.000
C52 Malignant neoplasm of vagina
0.000 0.992 0.008
S05 Injury of eye and orbit
0.008 0.992 0.000
Q63.8 Other specified congenital malformations of kidney
0.008 0.992 0.000
Q60.2 Renal agenesis, unspecified
0.008 0.992 0.000
R23 Other skin changes
0.007 0.993 0.000
S05.9 Injury of eye and orbit, part unspecified
0.007 0.993 0.000
S05.1 Contusion of eyeball and orbital tissues
0.007 0.993 0.000
C54.1 Endometrium
0.000 0.993 0.007
Q63.0 Accessory kidney
0.007 0.993 0.000
Q64.7 Other congenital malformations of bladder and urethra
0.007 0.993 0.000
Q62.5 Duplication of ureter
0.007 0.993 0.000
S72.20 Subtrochanteric fracture (closed)
0.007 0.993 0.000
Q60.6 Potter's syndrome
0.007 0.993 0.000
Q60.5 Renal hypoplasia, unspecified
0.007 0.993 0.000
Q60.4 Renal hypoplasia, bilateral
0.007 0.993 0.000
Q60.3 Renal hypoplasia, unilateral
0.007 0.993 0.000
Q60.1 Renal agenesis, bilateral
0.007 0.993 0.000
Z45.0 Adjustment and management of cardiac pacemaker
0.000 0.993 0.007
Q63.2 Ectopic kidney
0.007 0.993 0.000
C54.9 Corpus uteri, unspecified
0.000 0.993 0.007
C57 Malignant neoplasm of other and unspecified female genital organs
0.000 0.993 0.007
Q63.9 Congenital malformation of kidney, unspecified
0.006 0.993 0.000
Q63.3 Hyperplastic and giant kidney
0.006 0.993 0.000
S05.3 Ocular laceration without prolapse or loss of intraocular tissue
0.007 0.993 0.000
C58 Malignant neoplasm of placenta
0.000 0.993 0.006
Q64.3 Other atresia and stenosis of urethra and bladder neck
0.006 0.994 0.000
S02.20 Fracture of nasal bones (closed)
0.006 0.994 0.000
Q64.9 Congenital malformation of urinary system, unspecified
0.006 0.994 0.000
Q64.8 Other specified congenital malformations of urinary system
0.006 0.994 0.000
Q64.6 Congenital diverticulum of bladder
0.006 0.994 0.000
Q64.5 Congenital absence of bladder and urethra
0.006 0.994 0.000
Q64.4 Malformation of urachus
0.006 0.994 0.000
Q64.2 Congenital posterior urethral valves
0.006 0.994 0.000
Q64.1 Exstrophy of urinary bladder
0.006 0.994 0.000
Q64.0 Epispadias
0.006 0.994 0.000
H69.9 Eustachian tube disorder, unspecified
0.006 0.994 0.000
Q62.8 Other congenital malformations of ureter
0.006 0.994 0.000
Q62.7 Congenital vesico-uretero-renal reflux
0.006 0.994 0.000
Q62.6 Malposition of ureter
0.006 0.994 0.000
Q62.4 Agenesis of ureter
0.006 0.994 0.000
Q62.3 Other obstructive defects of renal pelvis and ureter
0.006 0.994 0.000
Q62.2 Congenital megaloureter
0.006 0.994 0.000
Q62.1 Atresia and stenosis of ureter
0.006 0.994 0.000
Q62.0 Congenital hydronephrosis
0.006 0.994 0.000
Q63.1 Lobulated, fused and horseshoe kidney
0.006 0.994 0.000
B34.4 Papovirus infection, unspecified
0.000 0.994 0.006
R23.0 Cyanosis
0.006 0.994 0.000
R23.4 Changes in skin texture
0.006 0.994 0.000
B34.3 Parvovirus infection, unspecified
0.000 0.994 0.006
B34.2 Coronavirus infection, unspecified
0.000 0.994 0.006
B34.1 Enterovirus infection, unspecified
0.000 0.994 0.006
B34.0 Adenovirus infection, unspecified
0.000 0.994 0.006
C54.8 Overlapping lesion of corpus uteri
0.000 0.994 0.006
C54.3 Fundus uteri
0.000 0.994 0.006
C54.2 Myometrium
0.000 0.994 0.006
C54.0 Isthmus uteri
0.000 0.994 0.006
S02.2 Fracture of nasal bones
0.006 0.994 0.000
S05.7 Avulsion of eye
0.006 0.994 0.000
S05.6 Penetrating wound of eyeball without foreign body
0.006 0.994 0.000
S05.5 Penetrating wound of eyeball with foreign body
0.006 0.994 0.000
S05.4 Penetrating wound of orbit with or without foreign body
0.006 0.994 0.000
R23.1 Pallor
0.006 0.994 0.000
C51 Malignant neoplasm of vulva
0.000 0.994 0.006
M94.88 Other specified disorders of cartilage (Other)
0.006 0.994 0.000
S05.2 Ocular laceration and rupture with prolapse or loss of intraocular tissue
0.005 0.994 0.000
M94.8 Other specified disorders of cartilage
0.005 0.995 0.000
S02 Fracture of skull and facial bones
0.005 0.995 0.000
C53 Malignant neoplasm of cervix uteri
0.000 0.995 0.005
M94.86 Other specified disorders of cartilage (Lower leg)
0.005 0.995 0.000
C57.0 Fallopian tube
0.000 0.995 0.005
S05.0 Injury of conjunctiva and corneal abrasion without mention of foreign body
0.005 0.995 0.000
C57.9 Female genital organ, unspecified
0.000 0.995 0.005
C57.8 Overlapping lesion of female genital organs
0.000 0.995 0.005
C57.7 Other specified female genital organs
0.000 0.995 0.005
C57.4 Uterine adnexa, unspecified
0.000 0.995 0.005
C57.3 Parametrium
0.000 0.995 0.005
C57.2 Round ligament
0.000 0.995 0.005
C57.1 Broad ligament
0.000 0.995 0.005
R16.1 Splenomegaly, not elsewhere classified
0.000 0.995 0.005
S02.3 Fracture of orbital floor
0.005 0.995 0.000
S02.21 Fracture of nasal bones (open)
0.005 0.995 0.000
B34.8 Other viral infections of unspecified site
0.000 0.995 0.005
T85.2 Mechanical complication of intraocular lens
0.005 0.995 0.000
S02.30 Fracture of orbital floor (closed)
0.005 0.995 0.000
M94.89 Other specified disorders of cartilage (Site unspecified)
0.005 0.995 0.000
S02.1 Fracture of base of skull
0.005 0.995 0.000
S02.8 Fractures of other skull and facial bones
0.005 0.995 0.000
H69 Other disorders of Eustachian tube
0.005 0.995 0.000
S02.6 Fracture of mandible
0.004 0.995 0.000
Q38-Q45 Other congenital malformations of the digestive system
0.004 0.996 0.000
S02.5 Fracture of tooth
0.004 0.996 0.000
Chapter XVII Congenital malformations, deformations and chromosomal abnormalities
0.004 0.996 0.000
S02.7 Multiple fractures involving skull and facial bones
0.004 0.996 0.000
C51.8 Overlapping lesion of vulva
0.000 0.996 0.004
C51.2 Clitoris
0.000 0.996 0.004
C51.1 Labium minus
0.000 0.996 0.004
R23.2 Flushing
0.004 0.996 0.000
M94.85 Other specified disorders of cartilage (Pelvic region and thigh)
0.004 0.996 0.000
Q87.4 Marfan's syndrome
0.004 0.996 0.000
R16.0 Hepatomegaly, not elsewhere classified
0.000 0.996 0.004
M75.1 Rotator cuff syndrome
0.004 0.996 0.000
Q87 Other specified congenital malformation syndromes affecting multiple systems
0.004 0.996 0.000
M94.87 Other specified disorders of cartilage (Ankle and foot)
0.004 0.996 0.000
M94.84 Other specified disorders of cartilage (Hand)
0.004 0.996 0.000
M94.83 Other specified disorders of cartilage (Forearm)
0.004 0.996 0.000
M94.82 Other specified disorders of cartilage (Upper arm)
0.004 0.996 0.000
M94.81 Other specified disorders of cartilage (Shoulder region)
0.004 0.996 0.000
M94.80 Other specified disorders of cartilage (Multiple sites)
0.004 0.996 0.000
S02.10 Fracture of base of skull (closed)
0.004 0.996 0.000
C51.0 Labium majus
0.000 0.996 0.004
E27.4 Other and unspecified adrenocortical insufficiency
0.004 0.996 0.000
Q38 Other congenital malformations of tongue, mouth and pharynx
0.004 0.996 0.000
C53.8 Overlapping lesion of cervix uteri
0.000 0.996 0.004
C53.1 Exocervix
0.000 0.996 0.004
Q43 Other congenital malformations of intestine
0.004 0.996 0.000
S03 Dislocation, sprain and strain of joints and ligaments of head
0.004 0.996 0.000
T85 Complications of other internal prosthetic devices, implants and grafts
0.004 0.996 0.000
M94 Other disorders of cartilage
0.004 0.996 0.000
S00-S09 Injuries to the head
0.004 0.996 0.000
H69.8 Other specified disorders of Eustachian tube
0.004 0.996 0.000
Q44 Congenital malformations of gallbladder, bile ducts and liver
0.004 0.996 0.000
Q80-Q89 Other congenital malformations
0.004 0.996 0.000
D25.1 Intramural leiomyoma of uterus
0.004 0.996 0.000
R16 Hepatomegaly and splenomegaly, not elsewhere classified
0.000 0.996 0.004
S02.80 Fractures of other skull and facial bones (closed)
0.004 0.996 0.000
S02.9 Fracture of skull and facial bones, part unspecified
0.004 0.996 0.000
S03.0 Dislocation of jaw
0.004 0.996 0.000
Q90-Q99 Chromosomal abnormalities, not elsewhere classified
0.004 0.996 0.000
S02.31 Fracture of orbital floor (open)
0.004 0.996 0.000
S02.60 Fracture of mandible (closed)
0.004 0.996 0.000
Q38.7 Pharyngeal pouch
0.004 0.996 0.000
C51.9 Vulva, unspecified
0.000 0.996 0.003
Q87.8 Other specified congenital malformation syndromes, not elsewhere classified
0.004 0.996 0.000
S02.50 Fracture of tooth (closed)
0.004 0.996 0.000
S02.11 Fracture of base of skull (open)
0.003 0.996 0.000
Q44.5 Other congenital malformations of bile ducts
0.004 0.996 0.000
Q40 Other congenital malformations of upper alimentary tract
0.004 0.996 0.000
S02.70 Multiple fractures involving skull and facial bones (closed)
0.003 0.996 0.000
K29.5 Chronic gastritis, unspecified
0.004 0.996 0.000
S72.2 Subtrochanteric fracture
0.004 0.996 0.000
H40.0 Glaucoma suspect
0.000 0.996 0.004
S02.81 Fractures of other skull and facial bones (open)
0.003 0.996 0.000
Q43.3 Congenital malformations of intestinal fixation
0.003 0.996 0.000
H69.0 Patulous Eustachian tube
0.003 0.996 0.000
S02.61 Fracture of mandible (open)
0.003 0.996 0.000
S03.2 Dislocation of tooth
0.003 0.996 0.000
M93.9 Osteochondropathy, unspecified
0.003 0.997 0.000
Q45 Other congenital malformations of digestive system
0.003 0.997 0.000
Q42 Congenital absence, atresia and stenosis of large intestine
0.003 0.997 0.000
Q41 Congenital absence, atresia and stenosis of small intestine
0.003 0.997 0.000
Q35-Q37 Cleft lip and cleft palate
0.003 0.997 0.000
S02.4 Fracture of malar and maxillary bones
0.003 0.997 0.000
S02.51 Fracture of tooth (open)
0.003 0.997 0.000
C53.9 Cervix uteri, unspecified
0.000 0.997 0.003
Q43.9 Congenital malformation of intestine, unspecified
0.003 0.997 0.000
Q30-Q34 Congenital malformations of the respiratory system
0.003 0.997 0.000
S02.71 Multiple fractures involving skull and facial bones (open)
0.003 0.997 0.000
M94.0 Chondrocostal junction syndrome [Tietze]
0.003 0.997 0.000
Q43.8 Other specified congenital malformations of intestine
0.003 0.997 0.000
C53.0 Endocervix
0.000 0.997 0.003
Q43.1 Hirschsprung's disease
0.003 0.997 0.000
Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
0.003 0.997 0.000
T85.5 Mechanical complication of gastro-intestinal prosthetic devices, implants and grafts
0.003 0.997 0.000
T85.1 Mechanical complication of implanted electronic stimulator of nervous system
0.003 0.997 0.000
Q87.5 Other congenital malformation syndromes with other skeletal changes
0.003 0.997 0.000
Q87.3 Congenital malformation syndromes involving early overgrowth
0.003 0.997 0.000
Q87.2 Congenital malformation syndromes predominantly involving limbs
0.003 0.997 0.000
Q87.1 Congenital malformation syndromes predominantly associated with short stature
0.003 0.997 0.000
R16.2 Hepatomegaly with splenomegaly, not elsewhere classified
0.000 0.997 0.003
Q83 Congenital malformations of breast
0.003 0.997 0.000
Q98 Other sex chromosome abnormalities, male phenotype, not elsewhere classified
0.003 0.997 0.000
S02.0 Fracture of vault of skull
0.003 0.997 0.000
Q85 Phakomatoses, not elsewhere classified
0.003 0.997 0.000
Q99 Other chromosome abnormalities, not elsewhere classified
0.003 0.997 0.000
Q96 Turner's syndrome
0.003 0.997 0.000
Q38.8 Other congenital malformations of pharynx
0.003 0.997 0.000
Q38.6 Other congenital malformations of mouth
0.003 0.997 0.000
Q38.5 Congenital malformations of palate, not elsewhere classified
0.003 0.997 0.000
Q38.4 Congenital malformations of salivary glands and ducts
0.003 0.997 0.000
Q38.3 Other congenital malformations of tongue
0.003 0.997 0.000
Q38.2 Macroglossia
0.003 0.997 0.000
Q38.1 Ankyloglossia
0.003 0.997 0.000
Q38.0 Congenital malformations of lips, not elsewhere classified
0.003 0.997 0.000
Q43.7 Persistent cloaca
0.003 0.997 0.000
Q43.6 Congenital fistula of rectum and anus
0.003 0.997 0.000
Q43.5 Ectopic anus
0.003 0.997 0.000
Q43.4 Duplication of intestine
0.003 0.997 0.000
Q43.2 Other congenital functional disorders of colon
0.003 0.997 0.000
Q10-Q18 Congenital malformations of eye, ear, face and neck
0.003 0.997 0.000
S03.5 Sprain and strain of joints and ligaments of other and unspecified parts of head
0.003 0.997 0.000
S03.4 Sprain and strain of jaw
0.003 0.997 0.000
S03.3 Dislocation of other and unspecified parts of head
0.003 0.997 0.000
S03.1 Dislocation of septal cartilage of nose
0.003 0.997 0.000
M94.3 Chondrolysis
0.003 0.997 0.000
M94.1 Relapsing polychondritis
0.003 0.997 0.000
Q86 Congenital malformation syndromes due to known exogenous causes, not elsewhere classified
0.003 0.997 0.000
Q84 Other congenital malformations of integument
0.003 0.997 0.000
Q81 Epidermolysis bullosa
0.003 0.997 0.000
Q80 Congenital ichthyosis
0.003 0.997 0.000
S08 Traumatic amputation of part of head
0.003 0.997 0.000
S07 Crushing injury of head
0.003 0.997 0.000
S04 Injury of cranial nerves
0.003 0.997 0.000
Q44.7 Other congenital malformations of liver
0.003 0.997 0.000
Q44.6 Cystic disease of liver
0.003 0.997 0.000
Q44.4 Choledochal cyst
0.003 0.997 0.000
Q44.3 Congenital stenosis and stricture of bile ducts
0.003 0.997 0.000
Q44.2 Atresia of bile ducts
0.003 0.997 0.000
Q44.1 Other congenital malformations of gallbladder
0.003 0.997 0.000
Q44.0 Agenesis, aplasia and hypoplasia of gallbladder
0.003 0.997 0.000
M94.2 Chondromalacia
0.003 0.997 0.000
Q40.3 Congenital malformation of stomach, unspecified
0.003 0.997 0.000
B25-B34 Other viral diseases
0.000 0.997 0.003
S02.91 Fracture of skull and facial bones, part unspecified (open)
0.003 0.997 0.000
M94.9 Disorder of cartilage, unspecified
0.003 0.997 0.000
Q97 Other sex chromosome abnormalities, female phenotype, not elsewhere classified
0.003 0.997 0.000
Q95 Balanced rearrangements and structural markers, not elsewhere classified
0.003 0.997 0.000
Q93 Monosomies and deletions from the autosomes, not elsewhere classified
0.003 0.997 0.000
Q92 Other trisomies and partial trisomies of the autosomes, not elsewhere classified
0.003 0.997 0.000
Q91 Edwards' syndrome and Patau's syndrome
0.003 0.997 0.000
Q90 Down's syndrome
0.003 0.997 0.000
S06 Intracranial injury
0.003 0.997 0.000
Q85.9 Phakomatosis, unspecified
0.003 0.997 0.000
T85.0 Mechanical complication of ventricular intracranial (communicating) shunt
0.003 0.997 0.000
Q00-Q07 Congenital malformations of the nervous system
0.003 0.997 0.000
M93 Other osteochondropathies
0.003 0.997 0.000
M94.08 Chondrocostal junction syndrome [Tietze]-Other
0.003 0.997 0.000
D12.4 Descending colon
0.000 0.997 0.003
H74.0 Tympanosclerosis
0.003 0.997 0.000
S72.21 Subtrochanteric fracture (open)
0.003 0.997 0.000
Q40.9 Congenital malformation of upper alimentary tract, unspecified
0.003 0.997 0.000
Q40.8 Other specified congenital malformations of upper alimentary tract
0.003 0.997 0.000
Q40.1 Congenital hiatus hernia
0.003 0.997 0.000
Q40.0 Congenital hypertrophic pyloric stenosis
0.003 0.997 0.000
Q98.4 Klinefelter's syndrome, unspecified
0.003 0.997 0.000
Q39 Congenital malformations of oesophagus
0.003 0.997 0.000
H90.5 Sensorineural hearing loss, unspecified
0.000 0.997 0.003
T85.9 Unspecified complication of internal prosthetic device, implant and graft
0.003 0.997 0.000
Z86.1 Personal history of infectious and parasitic diseases
0.000 0.997 0.003
Q65-Q79 Congenital malformations and deformations of the musculoskeletal system
0.003 0.997 0.000
S02.90 Fracture of skull and facial bones, part unspecified (closed)
0.003 0.997 0.000
Q83.1 Accessory breast
0.003 0.997 0.000
Q37 Cleft palate with cleft lip
0.003 0.997 0.000
H74.3 Other acquired abnormalities of ear ossicles
0.003 0.997 0.000
Q41.9 Congenital absence, atresia and stenosis of small intestine, part unspecified
0.003 0.997 0.000
Q41.8 Congenital absence, atresia and stenosis of other specified parts of small intestine
0.003 0.997 0.000
Q41.2 Congenital absence, atresia and stenosis of ileum
0.003 0.997 0.000
Q41.1 Congenital absence, atresia and stenosis of jejunum
0.003 0.997 0.000
Q41.0 Congenital absence, atresia and stenosis of duodenum
0.003 0.997 0.000
Q42.9 Congenital absence, atresia and stenosis of large intestine, part unspecified
0.003 0.997 0.000
Q42.8 Congenital absence, atresia and stenosis of other parts of large intestine
0.003 0.997 0.000
Q42.3 Congenital absence, atresia and stenosis of anus without fistula
0.003 0.997 0.000
Q42.2 Congenital absence, atresia and stenosis of anus with fistula
0.003 0.997 0.000
Q42.1 Congenital absence, atresia and stenosis of rectum without fistula
0.003 0.997 0.000
Q42.0 Congenital absence, atresia and stenosis of rectum with fistula
0.003 0.997 0.000
Q45.9 Congenital malformation of digestive system, unspecified
0.003 0.997 0.000
Q45.8 Other specified congenital malformations of digestive system
0.003 0.997 0.000
Q45.3 Other congenital malformations of pancreas and pancreatic duct
0.003 0.997 0.000
Q45.2 Congenital pancreatic cyst
0.003 0.997 0.000
Q45.1 Annular pancreas
0.003 0.997 0.000
Q45.0 Agenesis, aplasia and hypoplasia of pancreas
0.003 0.997 0.000
S06.1 Traumatic cerebral oedema
0.003 0.997 0.000
Q36 Cleft lip
0.003 0.997 0.000
Q35 Cleft palate
0.003 0.997 0.000
S02.41 Fracture of malar and maxillary bones (open)
0.003 0.997 0.000
Q40.2 Other specified congenital malformations of stomach
0.003 0.997 0.000
Q99.8 Other specified chromosome abnormalities
0.003 0.997 0.000
Q34 Other congenital malformations of respiratory system
0.003 0.997 0.000
Q33 Congenital malformations of lung
0.003 0.997 0.000
Q32 Congenital malformations of trachea and bronchus
0.003 0.997 0.000
Q31 Congenital malformations of larynx
0.003 0.997 0.000
Q30 Congenital malformations of nose
0.003 0.997 0.000
Q96.9 Turner's syndrome, unspecified
0.003 0.997 0.000
H71 Cholesteatoma of middle ear
0.003 0.997 0.000
M23.36 Other meniscus derangements (Other and unspecified lateral meniscus)
0.003 0.997 0.000
M94.09 Chondrocostal junction syndrome [Tietze]-Site unspec
0.002 0.997 0.000
M94.07 Chondrocostal junction syndrome [Tietze]-Ankle/foot
0.002 0.997 0.000
M94.06 Chondrocostal junction syndrome [Tietze]-Lower leg
0.002 0.997 0.000
M94.05 Chondrocostal junction syndrome [Tietze]-Pelvic/thigh
0.002 0.997 0.000
M94.04 Chondrocostal junction syndrome [Tietze]-Hand
0.002 0.997 0.000
M94.03 Chondrocostal junction syndrome [Tietze]-Forearm
0.002 0.997 0.000
M94.02 Chondrocostal junction syndrome [Tietze]-Upper arm
0.002 0.997 0.000
M94.01 Chondrocostal junction syndrome [Tietze]-Shldr region
0.002 0.997 0.000
M94.00 Chondrocostal junction syndrome [Tietze]-Mult sites
0.002 0.997 0.000
Q85.8 Other phakomatoses, not elsewhere classified
0.003 0.997 0.000
S06.0 Concussion
0.003 0.997 0.000
Q98.9 Sex chromosome abnormality, male phenotype, unspecified
0.002 0.997 0.000
Q98.8 Other specified sex chromosome abnormalities, male phenotype
0.002 0.997 0.000
Q98.7 Male with sex chromosome mosaicism
0.002 0.997 0.000
Q98.6 Male with structurally abnormal sex chromosome
0.002 0.997 0.000
Q98.5 Karyotype 47,XYY
0.002 0.997 0.000
Q98.3 Other male with 46,XX karyotype
0.002 0.997 0.000
Q98.2 Klinefelter's syndrome, male with 46,XX karyotype
0.002 0.997 0.000
Q98.1 Klinefelter's syndrome, male with more than two X chromosomes
0.002 0.997 0.000
Q98.0 Klinefelter's syndrome karyotype 47,XXY
0.002 0.997 0.000
Q89 Other congenital malformations, not elsewhere classified
0.002 0.997 0.000
S02.01 Fracture of vault of skull (open)
0.002 0.997 0.000
Q83.9 Congenital malformation of breast, unspecified
0.002 0.997 0.000
Q83.8 Other congenital malformations of breast
0.002 0.997 0.000
Q83.3 Accessory nipple
0.002 0.997 0.000
Q83.2 Absent nipple
0.002 0.997 0.000
Q83.0 Congenital absence of breast with absent nipple
0.002 0.997 0.000
Q85.1 Tuberous sclerosis
0.002 0.997 0.000
R39.1 Other difficulties with micturition
0.000 0.997 0.003
S06.10 Traumatic cerebral oedema (without open intracranial wound)
0.002 0.997 0.000
B27 Infectious mononucleosis
0.000 0.997 0.002
Q74 Other congenital malformations of limb(s)
0.003 0.997 0.000
Q99.9 Chromosomal abnormality, unspecified
0.002 0.997 0.000
Q99.2 Fragile X chromosome
0.002 0.997 0.000
Q99.1 46,XX true hermaphrodite
0.002 0.997 0.000
Q99.0 Chimera 46,XX/46,XY
0.002 0.997 0.000
M91-M94 Chondropathies
0.003 0.997 0.000
Q96.8 Other variants of Turner's syndrome
0.002 0.997 0.000
Q96.4 Mosaicism, 45,X/other cell line(s) with abnormal sex chromosome
0.002 0.997 0.000
Q96.3 Mosaicism, 45,X/46,XX or XY
0.002 0.997 0.000
Q96.2 Karyotype 46,X with abnormal sex chromosome, except iso (Xq)
0.002 0.997 0.000
Q96.1 Karyotype 46,X iso (Xq)
0.002 0.997 0.000
Q96.0 Karyotype 45,X
0.002 0.997 0.000
S06.4 Epidural haemorrhage
0.002 0.997 0.000
Q10 Congenital malformations of eyelid, lachrymal apparatus and orbit
0.002 0.997 0.000
Q14 Congenital malformations of posterior segment of eye
0.002 0.997 0.000
Q16 Congenital malformations of ear causing impairment of hearing
0.002 0.997 0.000
Q15 Other congenital malformations of eye
0.002 0.997 0.000
Q13 Congenital malformations of anterior segment of eye
0.002 0.997 0.000
Q11 Anophthalmos, microphthalmos and macrophthalmos
0.002 0.997 0.000
H74 Other disorders of middle ear and mastoid
0.003 0.997 0.000
M94.19 Relapsing polychondritis (Site unspecified)
0.002 0.997 0.000
M94.18 Relapsing polychondritis (Other)
0.002 0.997 0.000
M94.17 Relapsing polychondritis (Ankle and foot)
0.002 0.997 0.000
M94.16 Relapsing polychondritis (Lower leg)
0.002 0.997 0.000
M94.15 Relapsing polychondritis (Pelvic region and thigh)
0.002 0.997 0.000
M94.14 Relapsing polychondritis (Hand)
0.002 0.997 0.000
M94.13 Relapsing polychondritis (Forearm)
0.002 0.997 0.000
M94.12 Relapsing polychondritis (Upper arm)
0.002 0.997 0.000
M94.11 Relapsing polychondritis (Shoulder region)
0.002 0.997 0.000
M94.10 Relapsing polychondritis (Multiple sites)
0.002 0.997 0.000
M94.39 Chondrolysis (Site unspecified)
0.002 0.997 0.000
M94.38 Chondrolysis (Other)
0.002 0.997 0.000
M94.37 Chondrolysis (Ankle and foot)
0.002 0.997 0.000
M94.36 Chondrolysis (Lower leg)
0.002 0.997 0.000
M94.35 Chondrolysis (Pelvic region and thigh)
0.002 0.997 0.000
M94.34 Chondrolysis (Hand)
0.002 0.997 0.000
M94.33 Chondrolysis (Forearm)
0.002 0.997 0.000
M94.32 Chondrolysis (Upper arm)
0.002 0.997 0.000
M94.31 Chondrolysis (Shoulder region)
0.002 0.997 0.000
M94.30 Chondrolysis (Multiple sites)
0.002 0.997 0.000
Q80.9 Congenital ichthyosis, unspecified
0.002 0.997 0.000
Q80.8 Other congenital ichthyosis
0.002 0.997 0.000
Q80.4 Harlequin foetus
0.002 0.997 0.000
Q80.3 Congenital bullous ichthyosiform erythroderma
0.002 0.997 0.000
Q80.2 Lamellar ichthyosis
0.002 0.997 0.000
Q80.1 X-linked ichthyosis
0.002 0.997 0.000
Q80.0 Ichthyosis vulgaris
0.002 0.997 0.000
Q81.9 Epidermolysis bullosa, unspecified
0.002 0.997 0.000
Q81.8 Other epidermolysis bullosa
0.002 0.997 0.000
Q81.2 Epidermolysis bullosa dystrophica
0.002 0.997 0.000
Q81.1 Epidermolysis bullosa letalis
0.002 0.997 0.000
Q81.0 Epidermolysis bullosa simplex
0.002 0.997 0.000
Q84.9 Congenital malformation of integument, unspecified
0.002 0.997 0.000
Q84.8 Other specified congenital malformations of integument
0.002 0.997 0.000
Q84.6 Other congenital malformations of nails
0.002 0.997 0.000
Q84.5 Enlarged and hypertrophic nails
0.002 0.997 0.000
Q84.4 Congenital leukonychia
0.002 0.997 0.000
Q84.3 Anonychia
0.002 0.997 0.000
Q84.2 Other congenital malformations of hair
0.002 0.997 0.000
Q84.1 Congenital morphological disturbances of hair, not elsewhere classified
0.002 0.997 0.000
Q84.0 Congenital alopecia
0.002 0.997 0.000
Q86.8 Other congenital malformation syndromes due to known exogenous causes
0.002 0.997 0.000
Q86.2 Dysmorphism due to warfarin
0.002 0.997 0.000
Q86.1 Foetal hydantoin syndrome
0.002 0.997 0.000
Q86.0 Foetal alcohol syndrome (dysmorphic)
0.002 0.997 0.000
S04.9 Injury of unspecified cranial nerve
0.002 0.997 0.000
S04.8 Injury of other cranial nerves
0.002 0.997 0.000
S04.7 Injury of accessory nerve
0.002 0.997 0.000
S04.6 Injury of acoustic nerve
0.002 0.997 0.000
S04.5 Injury of facial nerve
0.002 0.997 0.000
S04.4 Injury of abducent nerve
0.002 0.997 0.000
S04.3 Injury of trigeminal nerve
0.002 0.997 0.000
S04.2 Injury of trochlear nerve
0.002 0.997 0.000
S04.1 Injury of oculomotor nerve
0.002 0.997 0.000
S04.0 Injury of optic nerve and pathways
0.002 0.997 0.000
S06.3 Focal brain injury
0.002 0.997 0.000
S07.9 Crushing injury of head, part unspecified
0.002 0.997 0.000
S07.8 Crushing injury of other parts of head
0.002 0.997 0.000
S07.1 Crushing injury of skull
0.002 0.997 0.000
S07.0 Crushing injury of face
0.002 0.997 0.000
S08.9 Traumatic amputation of unspecified part of head
0.002 0.997 0.000
S08.8 Traumatic amputation of other parts of head
0.002 0.997 0.000
S08.1 Traumatic amputation of ear
0.002 0.997 0.000
S08.0 Avulsion of scalp
0.002 0.997 0.000
T85.4 Mechanical complication of breast prosthesis and implant
0.002 0.997 0.000
M94.29 Chondromalacia (Site unspecified)
0.002 0.997 0.000
M94.28 Chondromalacia (Other)
0.002 0.997 0.000
M94.27 Chondromalacia (Ankle and foot)
0.002 0.997 0.000
M94.25 Chondromalacia (Pelvic region and thigh)
0.002 0.997 0.000
M94.24 Chondromalacia (Hand)
0.002 0.997 0.000
M94.23 Chondromalacia (Forearm)
0.002 0.997 0.000
M94.22 Chondromalacia (Upper arm)
0.002 0.997 0.000
M94.21 Chondromalacia (Shoulder region)
0.002 0.997 0.000
M94.20 Chondromalacia (Multiple sites)
0.002 0.997 0.000
R26.8 Other and unspecified abnormalities of gait and mobility
0.000 0.997 0.003
B33 Other viral diseases, not elsewhere classified
0.000 0.997 0.002
B30 Viral conjunctivitis
0.000 0.997 0.002
B26 Mumps
0.000 0.997 0.002
H70 Mastoiditis and related conditions
0.002 0.997 0.000
Q82 Other congenital malformations of skin
0.002 0.997 0.001
M94.99 Disorder of cartilage, unspecified (Site unspecified)
0.002 0.998 0.000
M94.98 Disorder of cartilage, unspecified (Other)
0.002 0.998 0.000
M94.97 Disorder of cartilage, unspecified (Ankle and foot)
0.002 0.998 0.000
M94.95 Disorder of cartilage, unspecified (Pelvic region and thigh)
0.002 0.998 0.000
M94.94 Disorder of cartilage, unspecified (Hand)
0.002 0.998 0.000
M94.93 Disorder of cartilage, unspecified (Forearm)
0.002 0.998 0.000
M94.92 Disorder of cartilage, unspecified (Upper arm)
0.002 0.998 0.000
M94.91 Disorder of cartilage, unspecified (Shoulder region)
0.002 0.998 0.000
M94.90 Disorder of cartilage, unspecified (Multiple sites)
0.002 0.998 0.000
Q90.9 Down's syndrome, unspecified
0.002 0.998 0.000
Q90.2 Trisomy 21, translocation
0.002 0.998 0.000
Q90.1 Trisomy 21, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q90.0 Trisomy 21, meiotic nondisjunction
0.002 0.998 0.000
Q91.7 Patau's syndrome, unspecified
0.002 0.998 0.000
Q91.6 Trisomy 13, translocation
0.002 0.998 0.000
Q91.5 Trisomy 13, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q91.4 Trisomy 13, meiotic nondisjunction
0.002 0.998 0.000
Q91.3 Edwards' syndrome, unspecified
0.002 0.998 0.000
Q91.2 Trisomy 18, translocation
0.002 0.998 0.000
Q91.1 Trisomy 18, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q91.0 Trisomy 18, meiotic nondisjunction
0.002 0.998 0.000
Q92.9 Trisomy and partial trisomy of autosomes, unspecified
0.002 0.998 0.000
Q92.8 Other specified trisomies and partial trisomies of autosomes
0.002 0.998 0.000
Q92.7 Triploidy and polyploidy
0.002 0.998 0.000
Q92.6 Extra marker chromosomes
0.002 0.998 0.000
Q92.5 Duplications with other complex rearrangements
0.002 0.998 0.000
Q92.4 Duplications seen only at prometaphase
0.002 0.998 0.000
Q92.3 Minor partial trisomy
0.002 0.998 0.000
Q92.2 Major partial trisomy
0.002 0.998 0.000
Q92.1 Whole chromosome trisomy, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q92.0 Whole chromosome trisomy, meiotic nondisjunction
0.002 0.998 0.000
Q93.9 Deletion from autosomes, unspecified
0.002 0.998 0.000
Q93.8 Other deletions from the autosomes
0.002 0.998 0.000
Q93.7 Deletions with other complex rearrangements
0.002 0.998 0.000
Q93.6 Deletions seen only at prometaphase
0.002 0.998 0.000
Q93.5 Other deletions of part of a chromosome
0.002 0.998 0.000
Q93.4 Deletion of short arm of chromosome 5
0.002 0.998 0.000
Q93.3 Deletion of short arm of chromosome 4
0.002 0.998 0.000
Q93.2 Chromosome replaced with ring or dicentric
0.002 0.998 0.000
Q93.1 Whole chromosome monosomy, mosaicism (mitotic nondisjunction)
0.002 0.998 0.000
Q93.0 Whole chromosome monosomy, meiotic nondisjunction
0.002 0.998 0.000
Q95.9 Balanced rearrangement and structural marker, unspecified
0.002 0.998 0.000
Q95.8 Other balanced rearrangements and structural markers
0.002 0.998 0.000
Q95.5 Individuals with autosomal fragile site
0.002 0.998 0.000
Q95.4 Individuals with marker heterochromatin
0.002 0.998 0.000
Q95.3 Balanced sex/autosomal rearrangement in abnormal individual
0.002 0.998 0.000
Q95.2 Balanced autosomal rearrangement in abnormal individual
0.002 0.998 0.000
Q95.1 Chromosome inversion in normal individual
0.002 0.998 0.000
Q95.0 Balanced translocation and insertion in normal individual
0.002 0.998 0.000
Q97.9 Sex chromosome abnormality, female phenotype, unspecified
0.002 0.998 0.000
Q97.8 Other specified sex chromosome abnormalities, female phenotype
0.002 0.998 0.000
Q97.3 Female with 46,XY karyotype
0.002 0.998 0.000
Q97.2 Mosaicism, lines with various numbers of X chromosomes
0.002 0.998 0.000
Q97.1 Female with more than three X chromosomes
0.002 0.998 0.000
Q97.0 Karyotype 47,XXX
0.002 0.998 0.000
Q12 Congenital lens malformations
0.002 0.998 0.000
H70.9 Mastoiditis, unspecified
0.002 0.998 0.000
H65-H75 Diseases of middle ear and mastoid
0.002 0.998 0.000
M94.26 Chondromalacia (Lower leg)
0.002 0.998 0.000
N80.1 Endometriosis of ovary
0.002 0.998 0.000
Q74.1 Congenital malformation of knee
0.002 0.998 0.000

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

The full results table can be downloaded from this page.