Abdominal pain
Symptom Information:
Symptom ID: | HPO:0002027 | ||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the abdomen(HPO:0001438) Abdominal symptom(HPO:0011458) Abdominal pain(HPO:0002027) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal signs and symptoms(MedDRA:10018012) Gastrointestinal and abdominal pains (excl oral and throat)(MedDRA:10017926) Abdominal pain(HPO:0002027) |
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Database Frequency: | 184 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
5-oxoprolinase deficiency | (Orphanet:33572) |
Acquired angioedema | (Orphanet:91385) |
Acquired epidermolysis bullosa | (Orphanet:46487) |
Acute intermittent porphyria | (Orphanet:79276) |
Adult Still's disease | (Orphanet:829) |
Adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency | (Orphanet:329314) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alpha heavy-chain disease | (Orphanet:100025) |
Alveolar echinococcosis | (Orphanet:284) |
Anisakiasis | (Orphanet:1070) |
Autoimmune hemolytic anemia | (Orphanet:98375) |
Autosomal dominant hypocalcemia | (Orphanet:428) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Behçet disease | (Orphanet:117) |
Benign recurrent intrahepatic cholestasis | (Orphanet:65682) |
Botulism | (Orphanet:1267) |
Budd-Chiari syndrome | (Orphanet:131) |
CELIAC ARTERY STENOSIS FROM COMPRESSION BY MEDIAN ARCUATE LIGAMENTOF DIAPHRAGM | (OMIM:116870) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CREST syndrome | (Orphanet:90290) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
Carcinoma of the gallbladder | (Orphanet:56044) |
Carney triad | (Orphanet:139411) |
Carney-Stratakis syndrome | (Orphanet:97286) |
Castleman disease | (Orphanet:160) |
Cholangiocarcinoma | (Orphanet:70567) |
Cholera | (Orphanet:173) |
Cholestasis - lymphedema | (Orphanet:1414) |
Choreoacanthocytosis | (Orphanet:2388) |
Chronic diarrhea due to guanylate cyclase 2C overactivity | (Orphanet:314373) |
Cogan syndrome | (Orphanet:1467) |
Congenital primary megaureter | (Orphanet:617) |
Congenital sucrase-isomaltase deficiency | (Orphanet:35122) |
Crimean-Congo hemorrhagic fever | (Orphanet:99827) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cushing disease | (Orphanet:96253) |
Cushing syndrome | (Orphanet:553) |
Cutaneous mastocytoma | (Orphanet:79455) |
Cutaneous mastocytosis | (Orphanet:66646) |
Cyclic neutropenia | (Orphanet:2686) |
Cystinosis | (Orphanet:213) |
Cystinuria | (Orphanet:214) |
Cystinuria type A | (Orphanet:93612) |
Cystinuria type B | (Orphanet:93613) |
Dengue fever | (Orphanet:99828) |
Dent disease type 1 | (Orphanet:93622) |
Desmoid tumor | (Orphanet:873) |
Desmoplastic small round cell tumor | (Orphanet:83469) |
Distomatosis | (Orphanet:1685) |
Dubin-Johnson syndrome | (Orphanet:234) |
ENTEROPATHY, PROTEIN-LOSING | (OMIM:226300) |
Ebola hemorrhagic fever | (Orphanet:319218) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erdheim-Chester disease | (Orphanet:35687) |
FAMILIAL MEDITERRANEAN FEVER | (OMIM:249100) |
FAMILIAL MEDITERRANEAN FEVER, AUTOSOMAL DOMINANT | (OMIM:134610) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial advanced sleep-phase syndrome | (Orphanet:164736) |
Familial hypomagnesemia - hypercalciuria - nephrocalcinosis | (Orphanet:31043) |
Familial progressive cardiac conduction defect | (Orphanet:871) |
Focal dermal hypoplasia | (Orphanet:2092) |
Foodborne botulism | (Orphanet:228371) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized juvenile polyposis/juvenile polyposis coli | (Orphanet:329971) |
Giant cell arteritis | (Orphanet:397) |
Gitelman syndrome | (Orphanet:358) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Granulomatosis with polyangiitis | (Orphanet:900) |
HERMANSKY-PUDLAK SYNDROME 1 | (OMIM:203300) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hemochromatosis, type 2A | (OMIM:602390) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary angioedema | (Orphanet:91378) |
Hereditary angioedema type 1 | (Orphanet:100050) |
Hereditary angioedema type 2 | (Orphanet:100051) |
Hereditary chronic pancreatitis | (Orphanet:676) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary fructose intolerance | (Orphanet:469) |
Hermansky-Pudlak syndrome | (Orphanet:79430) |
Hermansky-Pudlak syndrome with pulmonary fibrosis | (Orphanet:231500) |
Hirschsprung disease | (Orphanet:388) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hydatidosis | (Orphanet:400) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperlipoproteinemia type 1 | (Orphanet:411) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Hypouricemia, renal, 2 | (OMIM:612076) |
INFLAMMATORY BOWEL DISEASE 1 | (OMIM:266600) |
INFLAMMATORY BOWEL DISEASE 11 | (OMIM:191390) |
Idiopathic acute eosinophilic pneumonia | (Orphanet:724) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Indolent systemic mastocytosis | (Orphanet:98848) |
Infant botulism | (Orphanet:178478) |
Infundibulopelvic stenosis - multicystic kidney | (Orphanet:1849) |
Isolated polycystic liver disease | (Orphanet:2924) |
Juvenile dermatomyositis | (Orphanet:93672) |
Juvenile idiopathic arthritis | (Orphanet:92) |
Juvenile polyposis syndrome | (Orphanet:2929) |
Kawasaki disease | (Orphanet:2331) |
Klatskin tumor | (Orphanet:99978) |
Lassa fever | (Orphanet:99824) |
Legionellosis | (Orphanet:549) |
Liposarcoma | (Orphanet:69078) |
Lyell syndrome | (Orphanet:537) |
Lymphangioleiomyomatosis | (Orphanet:538) |
MELAS | (Orphanet:550) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 4B (MNGIE TYPE) | (OMIM:613662) |
Malakoplakia | (Orphanet:556) |
Malignant atrophic papulosis | (Orphanet:679) |
Malignant peritoneal mesothelioma | (Orphanet:168811) |
Malonic aciduria | (Orphanet:943) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Mediterranean macrothrombocytopenia | (Orphanet:101022) |
Menetrier disease | (Orphanet:2494) |
Microscopic polyangiitis | (Orphanet:727) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Muckle-Wells syndrome | (Orphanet:575) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
Myxoid/round cell liposarcoma | (Orphanet:99967) |
NEUROBLASTOMA, SUSCEPTIBILITY TONEUROBLASTOMA, SUSCEPTIBILITY TO, 1, INCLUDED | (OMIM:256700) |
NLRP12-associated hereditary periodic fever syndrome | (Orphanet:247868) |
Nephroblastoma | (Orphanet:654) |
Nephronophthisis 1 | (OMIM:256100) |
Neuroblastoma | (Orphanet:635) |
Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
Nodular non-suppurative panniculitis | (Orphanet:33577) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Oculogastrointestinal muscular dystrophy | (Orphanet:1876) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Ovarian hyperstimulation syndrome | (Orphanet:64739) |
PAROXYSMAL NOCTURNAL HEMOGLOBINURIA 2 | (OMIM:615399) |
PELGER-HUET-LIKE ANOMALY AND EPISODIC FEVER WITH ABDOMINAL PAIN | (OMIM:260570) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Peritoneal cystic mesothelioma | (Orphanet:168816) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Polymyositis | (Orphanet:732) |
Porphyria | (Orphanet:738) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Porphyria variegata | (Orphanet:79473) |
Primary effusion lymphoma | (Orphanet:48686) |
Primary familial polycythemia | (Orphanet:90042) |
Primary intestinal lymphangiectasia | (Orphanet:90362) |
Primary peritoneal carcinoma | (Orphanet:168829) |
Pseudomyxoma peritonei | (Orphanet:26790) |
Reactive arthritis | (Orphanet:29207) |
Rhabdoid tumor | (Orphanet:69077) |
Rheumatic fever | (Orphanet:3099) |
Rotor syndrome | (Orphanet:3111) |
SAPHO syndrome | (Orphanet:793) |
Scheie syndrome | (Orphanet:93474) |
Scleroderma | (Orphanet:801) |
Scrub typhus | (Orphanet:83317) |
Sino-auricular heart block | (Orphanet:1260) |
Sitosterolemia | (Orphanet:2882) |
Small cell carcinoma of the bladder | (Orphanet:284400) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Systemic capillary leak syndrome | (Orphanet:188) |
Systemic mastocytosis | (Orphanet:2467) |
Systemic-onset juvenile idiopathic arthritis | (Orphanet:85414) |
TRAPS syndrome | (Orphanet:32960) |
Tropical pancreatitis | (Orphanet:103918) |
Typhoid | (Orphanet:99745) |
Viral hemorrhagic fever | (Orphanet:341) |
Vitamin B12-unresponsive methylmalonic acidemia type mut- | (Orphanet:79312) |
Waardenburg-Shah syndrome | (Orphanet:897) |
Whipple disease | (Orphanet:3452) |
Williams syndrome | (Orphanet:904) |
Wolman disease | (Orphanet:75233) |
Yellow fever | (Orphanet:99829) |