Abdominal pain

Symptom Information:

Symptom ID: HPO:0002027
Synonyms:
Acute Abdominal pain [Orphanet:27300]
Acute abdominal pain (finding) [Orphanet:27300]
Acute abdominal pain [Orphanet:27300]
Abdominal pain [OMIM:Abdominal pain]
Acute abdominal pain/colic [Orphanet:27300]
Abdominal pain [MedDRA:10000081]
Abd. pain [MedDRA:10000081]
Abdo pain [MedDRA:10000081]
Abdominal colic [MedDRA:10000081]
Abdominal cramp [MedDRA:10000081]
Abdominal cramps [MedDRA:10000081]
Abdominal crampy pains [MedDRA:10000081]
Abdominal pain generalised [MedDRA:10000081]
Abdominal pain localised [MedDRA:10000081]
Abdominal pain NOS [MedDRA:10000081]
Belly ache [MedDRA:10000081]
Central abdominal pain [MedDRA:10000081]
Colic [MedDRA:10000081]
Colic abdominal [MedDRA:10000081]
Colicky [MedDRA:10000081]
Cramp abdominal [MedDRA:10000081]
Duodenal ulcer-type symptoms [MedDRA:10000081]
Griping abdomen [MedDRA:10000081]
Griping abdominal [MedDRA:10000081]
Pain abdo [MedDRA:10000081]
Pain abdominal [MedDRA:10000081]
Tummy ache [MedDRA:10000081]
Abdominal pain aggravated [MedDRA:10000081]
Spleen pain [MedDRA:10000081]
Periumbilical pain [MedDRA:10000081]
Abdominal pain generalized [MedDRA:10000081]
Abdominal pain localized [MedDRA:10000081]
Functional abdominal pain [MedDRA:10000081]
Postprandial pain [MedDRA:10000081]
Peritoneal pain [MedDRA:10000081]
Chronic abdominal pain [MedDRA:10000081]
Abdominal pain (HCP) [OMIM:Abdominal pain (HCP)]
Abdominal pain (in some patients) [OMIM:Abdominal pain (in some patients)]
Abdominal pain (in some) [OMIM:Abdominal pain (in some)]
Abdominal pain. [OMIM:Abdominal pain.]
Colic [OMIM:Colic]
Colic abdominal [MedDRA:10009882]
Colic [Orphanet:27300]
Abdominal colic (finding) [Orphanet:27300]
Colicky pain (finding) [Orphanet:27300]
Abdominal colic [Orphanet:27300]
Quality:
Cross references:
Orphanet:27300 "Acute abdominal pain/colic" [Orphanet:27300]
OMIM: "Abdominal pain" [OMIM:Abdominal pain]
OMIM: "Abdominal pain (HCP)" [OMIM:Abdominal pain (HCP)]
OMIM: "Abdominal pain (in some patients)" [OMIM:Abdominal pain (in some patients)]
OMIM: "Abdominal pain (in some)" [OMIM:Abdominal pain (in some)]
OMIM: "Abdominal pain." [OMIM:Abdominal pain.]
OMIM: "Colic" [OMIM:Colic]
UMLS:C0740577 "Acute abdominal pain" [Orphanet:27300]
UMLS:C0232488 "Abdominal colic" [Orphanet:27300]
Is a (Direct Parents):
HPO         Abdominal symptom
MedDRA Gastrointestinal and abdominal pains (excl oral and throat)
Orphanet Functional anomalies of the digestive system
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)
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)
Beh├žet 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)