Abdominal pain

Basic details

Preferred term: Abdominal pain
Alt. terms: pain in abdominal region

HPO term: Abdominal pain
HPO code: HP:0002027

GenIA ID: 800
Last updated on: 2021-12-10 17:55:48

Cross ref. with other ontologies

NCIT: C26682
MESH: D015746
EFO: -
OAE:0000402
SNOMEDCT: -
ICD10: -

Description

An unpleasant sensation characterized by physical discomfort (such as pricking, throbbing, or aching) and perceived to originate in the abdomen.

Hierarchical classification

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101717 F 210260tree icon 7 Caucasian Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration PMID:25329329 [Fam.C:II.3(C.II.3)]; PMID:29729943 [Fam.C:II.3(C.II.3 (19))]; PMID:27418640 [P16(5)]
101757 M 210026 - North American Abdominal pain Immunodeficiency, common variable, 8 PMID:26768763 [Fam.605:P14]; PMID:26206937 [P3]
101802 F 211221tree icon - German Abdominal pain NFKB1 insufficiency PMID:33995346 [Fam.A:III.2(Pat2)]; PMID:150198 [Fam.DV:III.2(528)]; PMID:36105815 [Fam.Y350C:III.2(Y350C/2)]
102154 U 214596 - Armenian Abdominal pain Familial Cold Autoinflammatory Syndrome 2 PMID:21538323 [P1]
102155 U 214597 - Italian Abdominal pain Familial Cold Autoinflammatory Syndrome 2 PMID:21538323 [P2]
102984 F 215074tree icon 16 European/American Abdominal pain Immunodeficiency 97 PMID:31554793 [A.1(II.1)]
103288 F 215113tree icon 20 Hungarian Abdominal pain Immunodeficiency 82 with systemic inflammation PMID:33782605 [Fam.3:II.1(P4)]
103542 M 215156tree icon 5 Mexican Abdominal pain ARPC1B deficiency PMID:36708766 [Fam.C:II.3(P5)]
103731 F 215232tree icon 17 Georgian Jewish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552285 [Fam.A:III.3(A-III-3)]
103741 F 215233tree icon 0 Georgian Jewish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552285 [Fam.B:III.3(B-III-3)]
103744 F 215233tree icon 0 Georgian Jewish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552285 [Fam.B:III.6(B-III-6)]
103745 M 215234tree icon 7 Georgian Jewish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552285 [Fam.C:II.3(C-II-3)]
103773 F 215236tree icon - Georgian Jewish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552285 [Fam.E:II.2(E-II-2)]
103820 M 215254tree icon 15 French Acute abdomen Adenosine deaminase 2 deficiency PMID:25278816 [Fam.F785:II.5(P1)]
103855 F 215262tree icon - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552284 [Fam.7:II.1(P7)]; PMID:26233953 [Fam.F2:II.2(P2)]
103858 M 215262tree icon - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552284 [Fam.7:II.2(P8)]; PMID:26233953 [Fam.F2:II.1(P3)]
103859 M 215263tree icon - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:24552284 [Fam.8:II.1(P9)]; PMID:26233953 [Fam.F4:P5]
103880 F 215269tree icon 1 Finnish Abdominal pain Infantile-Onset Multisystem Autoimmune Disease 1 PMID:25038750 [P5]; PMID:25349174 [Fam.1:II.4(Patient 1)]
104229 F 215420tree icon 42 German Abdominal pain Polycystic liver disease 5 with or without kidney disease PMID:36478640 [II.3(II.3)]
104237 M 215421tree icon - European/American Abdominal pain Systemic early-onset autoinflammation, vasculitis and hepatopathy PMID:36122175 [ref.8]; PMID:36932076 [P1(II.3)]; GRID:000818 [Patient]; GRID:000819 [pt.1]
104296 M 215449tree icon 2 Chinese (China) Abdominal pain Hyper-IgE recurrent infection syndrome 1 PMID:21107604 [Case(II.1)]
104351 M 215490 10 Caucasian Abdominal pain Hyper-IgE recurrent infection syndrome 1 PMID:26292779 [H1]
104352 F 215491 13 Caucasian Abdominal pain Hyper-IgE recurrent infection syndrome 1 PMID:26292779 [H2]
104392 F 215520tree icon - French Abdominal pain Systemic early-onset autoinflammation, vasculitis and hepatopathy PMID:36122175 [Patient]
104395 M 215521tree icon - British Abdominal pain Systemic early-onset autoinflammation, vasculitis and hepatopathy PMID:36122175 [ref.9]; PMID:36932076 [P2(II.1)]; GRID:000819 [pt.2]
104410 M 215525tree icon 4 Japanese Abdominal pain Early-onset atopic inflammation PMID:36538978 [Patient(II.2)]
104453 F 215530tree icon 15 European Abdominal pain Early-onset atopic inflammation PMID:36884218 [Fam.D:II.1(P5)]
104554 M 215551tree icon - Pakistani Abdominal pain Autoinflammation, panniculitis, and dermatosis syndrome PMID:27523608 [Fam.1:V.2(V:2)]; PMID:27559085 [Fam.1:V.2(P1)]; PMID:35587511 [Fam.G:II.2(4)]; PMID:34797715 [P1]; PMID:38914362 [Fam.A:V.2(023)]
104612 M 215557tree icon 7 Greek Abdominal pain Autoinflammation, panniculitis, and dermatosis syndrome PMID:35170849 [Patient(II.2)]; PMID:38914362 [Fam.F:II.2(069)]
104639 F 215562 3 Iraqi Abdominal pain Immunodeficiency 91 and hyperinflammation PMID:33872655 [Fam.A:II.2(P1.2)]
104886 F 215613tree icon 13 Caucasian Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.G:III.1(G.III.1 (26))]; PMID:25367873 [Fam.1:III.6(III.6)]
105034 F 215628tree icon 17 Finnish Abdominal pain Infantile-Onset Multisystem Autoimmune Disease 1 PMID:25349174 [Fam.3:II.1(Patient 3)]
105057 F 215635tree icon - German Abdominal pain NFKB1 insufficiency PMID:32278790 [S.I.1]; PMID:29403474 [Patient 1 (8)]; PMID:27365489 [Fam.1:II.1(Pat.1)]; PMID:150198 [Fam.AE:II.1(121)]
105172 M 215659 2 Caucasian Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.T:II.1(T.II.1 (48))]; PMID:27102614 [Fam.A:II.1(1)]
105212 F 215666tree icon - Finnish Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.F1:II.4(II.4)]; PMID:29403474 [Fam.1 (9):II.4(F1.II-4)]; PMID:28115215 [Fam.1:II.4(F1.II-4)]; PMID:150198 [Fam.AQ:II.4(174)]; PMID:36356849 [Fam.6:II.4(F6:II:4)]; PMID:36105815 [Fam.H67R:II.4(H67R/2)]
105219 F 215666tree icon 6 Finnish Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.F1:III.7(III.7)]; PMID:29403474 [Fam.1 (9):III.7(F1.III-7)]; PMID:28115215 [Fam.1:III.7(F1.III-7)]; PMID:150198 [Fam.AQ:III.7(181)]; PMID:36356849 [Fam.6:III.7(F6:III:7)]; PMID:36105815 [Fam.H67R:III.7(H67R/6)]
105220 F 215666tree icon 19,24 Finnish Abdominal cramps,Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.F1:III.8(III.8)]; PMID:29403474 [Fam.1 (9):III.8(F1.III-8)]; PMID:28115215 [Fam.1:III.8(F1.III-8)]; PMID:150198 [Fam.AQ:III.8(182)]; PMID:36356849 [Fam.6:III.8(F6:III:8)]; PMID:36105815 [Fam.H67R:III.8(H67R/7)]
105222 F 215666tree icon - Finnish Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.F1:IV.1(IV.1)]; PMID:29403474 [Fam.1 (9):IV.2(F1.IV-2)]; PMID:28115215 [Fam.1:IV.2(F1.IV-2)]; PMID:150198 [Fam.AQ:IV.2(184)]; PMID:36356849 [Fam.6:IV.2(F6:IV:2)]; PMID:36105815 [Fam.H67R:IV.2(H67R/9)]
105273 F 215682 18 North American Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration GRID:000111 [Patient(I.1)]
105317 M 215692tree icon - European Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.J:III.2(III.2)]; PMID:29477724 [Fam.J:III.2(III:2)]; PMID:150198 [Fam.BD:III.2(277)]
105423 M 215765tree icon - Caucasian Abdominal pain NFKB1 insufficiency PMID:150198 [Fam.BO:II.2(308)]; PMID:30761159 [Fam.1:II.2(patient)]
105428 M 215766tree icon 2 Admixed Abdominal pain Adenosine deaminase 2 deficiency PMID:26867732 [Fam.F:II.2(P9)]; PMID:25457153 [Fam.1:II.3(P2)]; PMID:25075846 [Fam.1:II.3(younger-sib)]
105549 F 215801 - Caucasian Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration PMID:29200144 [Fam.A:IV.1(P1)]
105640 F 215830 1 Abdominal pain Immunodeficiency, common variable, 8 PMID:34368306 [Patient 2]
105690 F 215840tree icon - Caucasian Abdominal pain NFKB1 insufficiency PMID:32278790 [Fam.BL:II.1(II.1)]; PMID:150198 [Fam.CE:II.1(417)]; PMID:36105815 [Fam.H67Y:II.1(H67Y/2)]
105746 M 215851tree icon - Finnish Abdominal pain Immunodeficiency, common variable, 14 PMID:34451894 [Patient(II.2)]; PMID:37876937 [Fam.C:II.2(C.1)]
105778 F 215871tree icon 7 Spanish Abdominal pain NFKB1 insufficiency PMID:32278790 [CB.I.1]; PMID:150198 [Fam.DM:II.1(472)]; PMID:36105815 [Fam.G386R:II.1(G386R/1)]
106263 M 215978tree icon 14 European/American Abdominal pain NFKB1 insufficiency PMID:150198 [Fam.FY:II.3(786)]; PMID:38593810 [Fam.5:II.3(F5.II-3)]
106304 M 215981tree icon - Chinese (China) Abdominal pain NFKB1 insufficiency PMID:150198 [Fam.FO:II.5(717)]; PMID:36571238 [Fam.1:II.5(II:5[P1])]
106315 F 215771tree icon 2 Caucasian Abdominal pain NFKB1 insufficiency PMID:150198 [Fam.BV:III.1(346)]; PMID:36105815 [Fam.R157P:III.1(S8's daugther)]
106323 M 215985tree icon 16 Abdominal pain NFKB1 insufficiency PMID:150198 [Fam.EZ:II.1(612)]; PMID:36105815 [Fam.R284P:II.1(R284P/1)]
106358 M 216000 16 Abdominal pain CTLA4 haploinsufficiency with autoimmune infiltration PMID:31993940 [Patient(II.1)]
106363 F 216001tree icon 3 Argentinian Abdominal pain Immunodeficiency 117 PMID:36736301 [Fam.A:II.1(P1)]
106479 M 216032 - Egyptian Abdominal pain Immunodeficiency, common variable, 8 PMID:32506362 [P14(II.1)]
106481 F 216034 - Egyptian Abdominal pain Immunodeficiency, common variable, 8 PMID:32506362 [Fam.216032:II.3(P16)]
106555 M 216078tree icon - Caucasian Abdominal pain Adenosine deaminase 2 deficiency PMID:26867732 [Fam.A:II.1(P1)]; PMID:25075845 [Fam.1:II.2(Young-bro)]
106577 F 216081tree icon - Caucasian Abdominal pain Adenosine deaminase 2 deficiency PMID:26867732 [Fam.D:II.2(P6)]
106581 F 216082tree icon - Caucasian Abdominal pain Adenosine deaminase 2 deficiency PMID:26867732 [Fam.E:II.1(P7)]
106851 F 216170 - South Asian Abdominal pain Adenosine deaminase 2 deficiency PMID:31008556 [Fam.2:P2]
106875 F 216179 0 Japanese Abdominal pain Adenosine deaminase 2 deficiency PMID:33529688 [Fam.4:II.3(P6)]
106888 M 216182tree icon 2 Caucasian Abdominal pain Adenosine deaminase 2 deficiency PMID:28830446 [P1(II.1)]
106889 M 216182tree icon 3 Caucasian Abdominal pain Adenosine deaminase 2 deficiency PMID:28830446 [Fam.P1:II.2(P2)]
107142 F 216359 - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:26233953 [Fam.F1:P1]
107143 M 216360 - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:26233953 [Fam.F3:P4]
107144 F 216361 - Turkish Abdominal pain Adenosine deaminase 2 deficiency PMID:26233953 [Fam.F5:P6]
107224 F 216380 17 Singaporean Abdominal pain Adenosine deaminase 2 deficiency PMID:27069017 [Patient]

*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).