Increased IgA levels

Basic details

Preferred term: Increased IgA levels
Alt. terms: Elevated serum IgA level | Increased circulating IgA level | Elevated IgA | IgA hypergammaglobulinemia

HPO term: Increased circulating IgA level
HPO code: HP:0003261

GenIA ID: 759
Last updated on: 2021-12-10 17:55:48

Cross ref. with other ontologies

NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -

Description

An abnormally increased level of immunoglobulin A in blood.

Hierarchical classification

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101062 M 212603tree icon - South Asian Increased IgA levels ARPC1B deficiency PMID:28368018 [Fam.1:II.1(P1)]; PMID:30771411 [P9]; PMID:34673575 [Fam.1:II.1(P1)]
101587 M 212604tree icon - Scottish Increased IgA levels ARPC1B deficiency PMID:28368018 [Fam.2:II.1(P2)]; PMID:30771411 [P10(II.1)]; PMID:34673575 [Fam.2:II.3(P2)]
101591 M 212604tree icon - Scottish Increased IgA levels ARPC1B deficiency PMID:28368018 [Fam.2:II.2(P3)]; PMID:30771411 [Fam.P10:II.2(P11)]; PMID:34673575 [Fam.2:II.2(P3)]
101592 M 212605tree icon 0 Moroccan Increased IgA levels ARPC1B deficiency PMID:27965109 [P1(II.1)]; PMID:30771411 [P1]; PMID:31710310 [Patient]; PMID:32499645 [Case 1]; PMID:34135903 [Patient]
101596 M 212618tree icon 1 Jewish Increased IgA levels ARPC1B deficiency PMID:29127144 [P1(II.1)]
101597 M 212618tree icon 0 Jewish Increased IgA levels ARPC1B deficiency PMID:29127144 [Fam.P1:II.10(P2)]; PMID:30254128 [P7]; PMID:35767111 [P6]
101601 M 212619tree icon - Italian Increased IgA levels ARPC1B deficiency PMID:30254128 [Fam.A:II.1(P1)]; PMID:30771411 [P2]; PMID:35967303 [Pt2]; PMID:35767111 [P2]
101604 M 212620tree icon 4 Italian Increased IgA levels ARPC1B deficiency PMID:30254128 [Fam.B:II.1(P2)]; PMID:30771411 [P3]; PMID:35967303 [Pt1]; PMID:35767111 [P1]
101608 M 212621tree icon - Canadian Increased IgA levels ARPC1B deficiency PMID:30254128 [Fam.C:II.1(P3)]; PMID:16019263 [case]; PMID:35967303 [Pt3]
101631 F 212624tree icon - Turkish Increased IgA levels ARPC1B deficiency PMID:30254128 [Fam.F:II.1(P6)]
101652 M 212629tree icon 3 Nepalese Increased IgA levels ARPC1B deficiency PMID:30771411 [P4(II.1)]
101667 M 212631tree icon 6 Moroccan Increased IgA levels ARPC1B deficiency PMID:30771411 [P6(II.2)]; PMID:35767111 [P5]
101671 F 212632tree icon 4 Iranian Increased IgA levels ARPC1B deficiency PMID:30771411 [P7(IV.8)]; PMID:31710310 [Patient 2]
101674 F 212632tree icon 9 Iranian Increased IgA levels ARPC1B deficiency PMID:30771411 [Fam.P7:V.1(P8)]
101687 F 212635tree icon 1 Nepalese Increased IgA levels ARPC1B deficiency PMID:30771411 [P12(II.1)]
101690 F 212636tree icon 4 Jordanian Increased IgA levels ARPC1B deficiency PMID:30771411 [P13(IV.5)]
101693 M 212637tree icon 8 Nepalese Increased IgA levels ARPC1B deficiency PMID:30771411 [P14(II.1)]
102216 F 214916tree icon 3 Belgian Hypergammaglobulinaemia Severe congenital neutropenia 11 PMID:32325141 [Patient(II.1)]
102239 F 214923tree icon - Brasilian Increased IgA levels ARPC1B deficiency GRID:000604 [case(II.2)]; PMID:37349293 [Fam.B:II.1(Patient)]
102245 M 214924tree icon 14 Afghanistani Increased IgA levels ARPC1B deficiency PMID:33679784 [Fam.II-6:II.1(II-1)]
102247 F 214924tree icon 10 Afghanistani Increased IgA levels ARPC1B deficiency PMID:33679784 [Fam.II-6:II.3(II-3)]
102250 M 214924tree icon 1 Afghanistani Increased IgA levels ARPC1B deficiency PMID:33679784 [II-6(II.6)]; PMID:35767111 [P7]
102258 M 214926tree icon 0 Mexican Increased IgA levels ARPC1B deficiency PMID:32683750 [case(II.3)]; PMID:36708766 [Fam.A:II.3(P2)]
102260 F 214926tree icon - Mexican Increased IgA levels ARPC1B deficiency PMID:32683750 [Fam.case:II.2(sister)]; PMID:36708766 [Fam.A:II.2(P1)]
102410 F 214947tree icon 1 South Asian Increased IgA levels Hyper-IgE recurrent infection syndrome 4B PMID:28747427 [Fam.A:II.3(P1)]
102865 F 214996tree icon 1 Italian Increased IgA levels ARPC1B deficiency | Hartnup disease PMID:35967303 [PtII-1(II.1)]; PMID:35967303 [PtII-1(II.1)]
102901 F 215008tree icon 0 Brasilian Hypergammaglobulinaemia T-cell immunodeficiency, congenital alopecia, and nail dystrophy PMID:35064468 [patient(II.2)]
103061 M 215095tree icon - Finnish Increased IgA levels Seizures, cortical blindness, microcephaly syndrome PMID:33662367 [Fam.F1:II.9(P2)]
103462 F 215132tree icon - Moroccan Increased IgA levels ARPC1B deficiency PMID:35767111 [P4(II.2)]
103538 F 215155tree icon - Mexican Increased IgA levels ARPC1B deficiency PMID:36708766 [Fam.B:II.2(P3)]
103541 M 215155tree icon 2 Mexican Increased IgA levels ARPC1B deficiency PMID:36708766 [Fam.B:II.1(P4)]
103542 M 215156tree icon - Mexican Increased IgA levels ARPC1B deficiency PMID:36708766 [Fam.C:II.3(P5)]
103547 M 215157tree icon 11 Mexican Increased IgA levels ARPC1B deficiency PMID:36708766 [Fam.D:II.4(P6)]
104268 M 215444tree icon - Ashkenazi Jewish Increased IgA levels Infantile-Onset Multisystem Autoimmune Disease 1 PMID:28153428 [Patient(II.2)]
104521 F 215538 - Gypsy Increased IgA levels ARPC1B deficiency PMID:31379835 [P3]
104522 F 215539 1 Gypsy Increased IgA levels ARPC1B deficiency PMID:31379835 [P4]
104540 M 215549tree icon -,- North African Hypergammaglobulinaemia,Increased IgA levels X-linked multisystem autoinflammatory disease with immune dysregulation PMID:36952639 [Fam.F:II.1(Patient F)]
104554 M 215551tree icon 3 Pakistani Increased IgA levels 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)]
104568 F 215551tree icon 0 Pakistani Increased IgA levels Autoinflammation, panniculitis, and dermatosis syndrome PMID:27523608 [Fam.1:IV.3(IV:3)]; PMID:32231246 [IV:3(IV.3)]; PMID:27559085 [Fam.1:IV.1(P4)]; PMID:38914362 [Fam.A:V.6(027)]
104570 F 215551tree icon 3 Pakistani Increased IgA levels Autoinflammation, panniculitis, and dermatosis syndrome PMID:27523608 [Fam.1:IV.4(IV:4)]; PMID:27559085 [Fam.1:IV.3(NA)]; PMID:38914362 [Fam.A:V.7(028)]
104580 F 215553tree icon - Turkish Increased IgA levels Autoinflammation, panniculitis, and dermatosis syndrome PMID:27559085 [Fam.3:II.1(P3)]; PMID:35587511 [Fam.H:II.1(3)]; PMID:34797715 [P3]; PMID:38914362 [Fam.C:II.1(039)]
104671 F 215568tree icon 6 Lebanese Increased IgA levels Severe early onset systemic inflammation and autoimmunity PMID:37349293 [Fam.1:II.1(P1)]
104678 F 215569tree icon - Iranian Increased IgA levels Severe early onset systemic inflammation and autoimmunity PMID:37349293 [Fam.2:II.2(P2)]
105025 F 215626tree icon - French Increased IgA levels Infantile-Onset Multisystem Autoimmune Disease 1 PMID:32392079 [P1]; PMID:29590538 [Patient]; PMID:35677041 [Pt8]
105350 M 215712 2 Omani Hypergammaglobulinaemia Immunodeficiency, common variable, 8 PMID:28690850 [P1]
105799 M 215881tree icon 1 Pakistani Increased IgA levels Combined immunodeficiency 41 PMID:32980423 [Fam.1:V.2(1.V.2)]; PMID:150198 [Fam.DS:V.2(506)]
106363 F 216001tree icon 3 Argentinian Increased IgA levels Immunodeficiency 117 PMID:36736301 [Fam.A:II.1(P1)]
106463 F 216023tree icon - Japanese Hypergammaglobulinaemia NFKB1 insufficiency PMID:150198 [Fam.FX:II.3(779)]; PMID:38514645 [Fam.1:II.3(proband)]
106642 F 216097 2 European Hypergammaglobulinaemia CTLA4 haploinsufficiency with autoimmune infiltration PMID:31396201 [Fam.:II.1(P1)]
106888 M 216182tree icon 10 Caucasian Hypergammaglobulinaemia Adenosine deaminase 2 deficiency PMID:28830446 [P1(II.1)]
106889 M 216182tree icon 4 Caucasian Hypergammaglobulinaemia Adenosine deaminase 2 deficiency PMID:28830446 [Fam.P1:II.2(P2)]
106932 M 216188tree icon 5 Jewish Hypergammaglobulinaemia Adenosine deaminase 2 deficiency PMID:25075848 [patient]; PMID:30139808 [Fam.1:II.5(P)]
107103 M 216335tree icon - Chinese (China) Increased IgA levels Infantile-Onset Multisystem Autoimmune Disease 1 PMID:35677041 [Pt1(II.2)]
107176 M 216369 - Hypergammaglobulinaemia T-cell LGL leukemia 1 PMID:26419508 [Patient 1]
107249 F 216398tree icon 2 Argentinian Increased IgA levels Infantile-Onset Multisystem Autoimmune Disease 1 PMID:35677041 [Pt7]; PMID:29378236 [Fam.1:Patient 1]
107252 M 216399tree icon 3 North American Increased IgA levels Infantile-Onset Multisystem Autoimmune Disease 1 PMID:29378236 [Fam.2:II.2(Patient 2)]

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