Oesophagitis

K20

Case/Control GWAS

GWAS of K20

Statistics

Case Control
11986 448220

Top SNP Information

Associated Phenotypes

ID Name Top Correlation
HP: 0000118 Phenotypic abnormality 3/20
HP: 0000152 Abnormality of head or neck 3/20
HP: 0000159 Abnormal lip morphology 2/20
HP: 0000234 Abnormality of the head 3/20
HP: 0000240 Abnormality of skull size 8/20
HP: 0000252 Microcephaly 9/20
HP: 0000370 Abnormality of the middle ear 4/20
HP: 0000417 Slender nose 8/20
HP: 0000486 Strabismus 5/20
HP: 0000492 Abnormal eyelid morphology 2/20
HP: 0000496 Abnormality of eye movement 3/20
HP: 0000504 Abnormality of vision 2/20
HP: 0000505 Visual impairment 3/20
HP: 0000549 Abnormal conjugate eye movement 4/20
HP: 0000598 Abnormality of the ear 6/20
HP: 0000707 Abnormality of the nervous system 1/20
HP: 0000924 Abnormality of the skeletal system 3/20
HP: 0000929 Abnormal skull morphology 2/20
HP: 0000940 Abnormal diaphysis morphology 3/20
HP: 0000944 Abnormality of the metaphysis 6/20
HP: 0001072 Thickened skin 1/20
HP: 0001133 Constriction of peripheral visual field 8/20
HP: 0001155 Abnormality of the hand 7/20
HP: 0001167 Abnormality of finger 8/20
HP: 0001172 Abnormal thumb morphology 7/20
HP: 0001298 Encephalopathy 4/20
HP: 0001367 Abnormal joint morphology 3/20
HP: 0001399 Hepatic failure 3/20
HP: 0001410 Decreased liver function 3/20
HP: 0001500 Broad finger 8/20
HP: 0001626 Abnormality of the cardiovascular system 2/20
HP: 0001679 Abnormal aortic morphology 10/20
HP: 0001760 Abnormality of the foot 3/20
HP: 0001850 Abnormality of the tarsal bones 4/20
HP: 0001877 Abnormal erythrocyte morphology 8/20
HP: 0001892 Abnormal bleeding 2/20
HP: 0001903 Anemia 7/20
HP: 0001939 Abnormality of metabolism/homeostasis 2/20
HP: 0002011 Morphological central nervous system abnormality 3/20
HP: 0002014 Diarrhea 6/20
HP: 0002020 Gastroesophageal reflux 12/20
HP: 0002031 Abnormal esophagus morphology 11/20
HP: 0002036 Hiatus hernia 12/20
HP: 0002043 Esophageal stricture 9/20
HP: 0002086 Abnormality of the respiratory system 2/20
HP: 0002087 Abnormality of the upper respiratory tract 2/20
HP: 0002088 Abnormal lung morphology 4/20
HP: 0002090 Pneumonia 1/20
HP: 0002103 Abnormality of the pleura 2/20
HP: 0002202 Pleural effusion 1/20
HP: 0002239 Gastrointestinal hemorrhage 6/20
HP: 0002242 Abnormal intestine morphology 2/20
HP: 0002244 Abnormality of the small intestine 5/20
HP: 0002376 Developmental regression 8/20
HP: 0002578 Gastroparesis 1/20
HP: 0002580 Volvulus 5/20
HP: 0002597 Abnormality of the vasculature 2/20
HP: 0002617 Dilatation 4/20
HP: 0002664 Neoplasm 1/20
HP: 0002672 Gastrointestinal carcinoma 5/20
HP: 0002715 Abnormality of the immune system 2/20
HP: 0002793 Abnormal pattern of respiration 2/20
HP: 0002813 Abnormality of limb bone morphology 4/20
HP: 0002814 Abnormality of the lower limb 4/20
HP: 0002817 Abnormality of the upper limb 5/20
HP: 0002883 Hyperventilation 6/20
HP: 0002973 Abnormality of the forearm 8/20
HP: 0002977 Aplasia/Hypoplasia involving the central nervous system 1/20
HP: 0003011 Abnormality of the musculature 1/20
HP: 0003028 Abnormality of the ankles 3/20
HP: 0003549 Abnormality of connective tissue 11/20
HP: 0004364 Abnormal circulating nitrogen compound concentration 2/20
HP: 0004386 Gastrointestinal inflammation 7/20
HP: 0004783 Duodenal polyposis 6/20
HP: 0004791 Esophageal ulceration 8/20
HP: 0004798 Recurrent infection of the gastrointestinal tract 1/20
HP: 0004879 Intermittent hyperventilation 7/20
HP: 0005089 Abnormal metaphyseal trabeculation 8/20
HP: 0005105 Abnormal nasal morphology 8/20
HP: 0005202 Helicobacter pylori infection 1/20
HP: 0005266 Intestinal polyp 4/20
HP: 0005484 Postnatal microcephaly 9/20
HP: 0005607 Abnormal tracheobronchial morphology 2/20
HP: 0005622 Broad long bones 8/20
HP: 0005918 Abnormal finger phalanx morphology 5/20
HP: 0005922 Abnormal hand morphology 9/20
HP: 0006009 Broad phalanx 9/20
HP: 0006368 Forearm reduction defects 8/20
HP: 0006554 Acute hepatic failure 3/20
HP: 0006749 Malignant gastrointestinal tract tumors 5/20
HP: 0006771 Duodenal adenocarcinoma 6/20
HP: 0007239 Congenital encephalopathy 8/20
HP: 0007364 Aplasia/Hypoplasia of the cerebrum 8/20
HP: 0007378 Neoplasm of the gastrointestinal tract 9/20
HP: 0009602 Abnormality of thumb phalanx 7/20
HP: 0009768 Broad phalanges of the hand 8/20
HP: 0009774 Triangular shaped phalanges of the hand 7/20
HP: 0010450 Esophageal stenosis 11/20
HP: 0010937 Abnormality of the nasal skeleton 8/20
HP: 0010939 Abnormality of the nasal bone 8/20
HP: 0010978 Abnormality of immune system physiology 3/20
HP: 0011004 Abnormal systemic arterial morphology 7/20
HP: 0011024 Abnormality of the gastrointestinal tract 7/20
HP: 0011028 Abnormality of blood circulation 2/20
HP: 0011029 Internal hemorrhage 2/20
HP: 0011121 Abnormality of skin morphology 3/20
HP: 0011297 Abnormal digit morphology 7/20
HP: 0011304 Broad thumb 8/20
HP: 0011314 Abnormality of long bone morphology 2/20
HP: 0011793 Neoplasm by anatomical site 1/20
HP: 0011804 Abnormal muscle physiology 1/20
HP: 0011805 Abnormal skeletal muscle morphology 2/20
HP: 0011842 Abnormality of skeletal morphology 3/20
HP: 0011844 Abnormal appendicular skeleton morphology 4/20
HP: 0012115 Hepatitis 8/20
HP: 0012130 Abnormal erythroid lineage cell morphology 8/20
HP: 0012252 Abnormal respiratory system morphology 3/20
HP: 0012288 Neoplasm of head and neck 11/20
HP: 0012303 Abnormal aortic arch morphology 1/20
HP: 0012443 Abnormality of brain morphology 3/20
HP: 0012531 Pain 2/20
HP: 0012639 Abnormal nervous system morphology 1/20
HP: 0012647 Abnormal inflammatory response 4/20
HP: 0012649 Increased inflammatory response 4/20
HP: 0012718 Morphological abnormality of the gastrointestinal tract 5/20
HP: 0012719 Functional abnormality of the gastrointestinal tract 6/20
HP: 0012759 Neurodevelopmental abnormality 2/20
HP: 0012848 Small intestinal stenosis 5/20
HP: 0020047 Abnormal myeloid cell morphology 8/20
HP: 0025015 Abnormal vascular morphology 13/20
HP: 0025032 Abnormality of digestive system physiology 1/20
HP: 0025085 Bloody diarrhea 6/20
HP: 0025142 Constitutional symptom 3/20
HP: 0025155 Abnormality of hepatobiliary system physiology 3/20
HP: 0025270 Abnormality of esophagus physiology 11/20
HP: 0030256 Small intestinal polyposis 6/20
HP: 0030526 Severe constriction of peripheral visual field 8/20
HP: 0030680 Abnormality of cardiovascular system morphology 1/20
HP: 0030962 Abnormal morphology of the great vessels 1/20
HP: 0031463 Esophageal squamous papilloma 8/20
HP: 0031703 Abnormal ear morphology 6/20
HP: 0032064 Gastrointestinal eosinophilia 3/20
HP: 0032180 Abnormal circulating metabolite concentration 1/20
HP: 0040064 Abnormality of limbs 3/20
HP: 0040068 Abnormality of limb bone 4/20
HP: 0040069 Abnormal lower limb bone morphology 6/20
HP: 0040070 Abnormal upper limb bone morphology 2/20
HP: 0040195 Decreased head circumference 9/20
HP: 0040273 Adenocarcinoma of the intestines 6/20
HP: 0040274 Adenocarcinoma of the small intestine 5/20
HP: 0100022 Abnormality of movement 3/20
HP: 0100491 Abnormality of lower limb joint 6/20
HP: 0100580 Barrett esophagus 12/20
HP: 0100633 Esophagitis 12/20
HP: 0100751 Esophageal neoplasm 11/20
HP: 0100790 Hernia 11/20
HP: 0100833 Neoplasm of the small intestine 6/20
HP: 0100867 Duodenal stenosis 6/20
HP: 0200008 Intestinal polyposis 4/20
HP: 0200123 Chronic hepatitis 6/20
HP: 0410019 Epigastric pain 3/20
HP: 0410151 Eosinophilic infiltration of the esophagus 20/20