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
TERM
Increased IgA levels
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101062 | M | 212603![]() |
- | 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 | 212604![]() |
- | 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 | 212604![]() |
- | 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 | 212605![]() |
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 | 212618![]() |
1 | Jewish | Increased IgA levels | ARPC1B deficiency | PMID:29127144 [P1(II.1)] |
101597 | M | 212618![]() |
0 | Jewish | Increased IgA levels | ARPC1B deficiency | PMID:29127144 [Fam.P1:II.10(P2)]; PMID:30254128 [P7]; PMID:35767111 [P6] |
101601 | M | 212619![]() |
- | Italian | Increased IgA levels | ARPC1B deficiency | PMID:30254128 [Fam.A:II.1(P1)]; PMID:30771411 [P2]; PMID:35967303 [Pt2]; PMID:35767111 [P2] |
101604 | M | 212620![]() |
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 | 212621![]() |
- | Canadian | Increased IgA levels | ARPC1B deficiency | PMID:30254128 [Fam.C:II.1(P3)]; PMID:16019263 [case]; PMID:35967303 [Pt3] |
101631 | F | 212624![]() |
- | Turkish | Increased IgA levels | ARPC1B deficiency | PMID:30254128 [Fam.F:II.1(P6)] |
101652 | M | 212629![]() |
3 | Nepalese | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P4(II.1)] |
101667 | M | 212631![]() |
6 | Moroccan | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P6(II.2)]; PMID:35767111 [P5] |
101671 | F | 212632![]() |
4 | Iranian | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P7(IV.8)]; PMID:31710310 [Patient 2] |
101674 | F | 212632![]() |
9 | Iranian | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [Fam.P7:V.1(P8)] |
101687 | F | 212635![]() |
1 | Nepalese | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P12(II.1)] |
101690 | F | 212636![]() |
4 | Jordanian | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P13(IV.5)] |
101693 | M | 212637![]() |
8 | Nepalese | Increased IgA levels | ARPC1B deficiency | PMID:30771411 [P14(II.1)] |
102216 | F | 214916![]() |
3 | Belgian | Hypergammaglobulinaemia | Severe congenital neutropenia 11 | PMID:32325141 [Patient(II.1)] |
102239 | F | 214923![]() |
- | Brasilian | Increased IgA levels | ARPC1B deficiency | GRID:000604 [case(II.2)]; PMID:37349293 [Fam.B:II.1(Patient)] |
102245 | M | 214924![]() |
14 | Afghanistani | Increased IgA levels | ARPC1B deficiency | PMID:33679784 [Fam.II-6:II.1(II-1)] |
102247 | F | 214924![]() |
10 | Afghanistani | Increased IgA levels | ARPC1B deficiency | PMID:33679784 [Fam.II-6:II.3(II-3)] |
102250 | M | 214924![]() |
1 | Afghanistani | Increased IgA levels | ARPC1B deficiency | PMID:33679784 [II-6(II.6)]; PMID:35767111 [P7] |
102258 | M | 214926![]() |
0 | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:32683750 [case(II.3)]; PMID:36708766 [Fam.A:II.3(P2)] |
102260 | F | 214926![]() |
- | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:32683750 [Fam.case:II.2(sister)]; PMID:36708766 [Fam.A:II.2(P1)] |
102410 | F | 214947![]() |
1 | South Asian | Increased IgA levels | Hyper-IgE recurrent infection syndrome 4B | PMID:28747427 [Fam.A:II.3(P1)] |
102865 | F | 214996![]() |
1 | Italian | Increased IgA levels | ARPC1B deficiency | Hartnup disease | PMID:35967303 [PtII-1(II.1)]; PMID:35967303 [PtII-1(II.1)] |
102901 | F | 215008![]() |
0 | Brasilian | Hypergammaglobulinaemia | T-cell immunodeficiency, congenital alopecia, and nail dystrophy | PMID:35064468 [patient(II.2)] |
103061 | M | 215095![]() |
- | Finnish | Increased IgA levels | Seizures, cortical blindness, microcephaly syndrome | PMID:33662367 [Fam.F1:II.9(P2)] |
103462 | F | 215132![]() |
- | Moroccan | Increased IgA levels | ARPC1B deficiency | PMID:35767111 [P4(II.2)] |
103538 | F | 215155![]() |
- | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:36708766 [Fam.B:II.2(P3)] |
103541 | M | 215155![]() |
2 | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:36708766 [Fam.B:II.1(P4)] |
103542 | M | 215156![]() |
- | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:36708766 [Fam.C:II.3(P5)] |
103547 | M | 215157![]() |
11 | Mexican | Increased IgA levels | ARPC1B deficiency | PMID:36708766 [Fam.D:II.4(P6)] |
104268 | M | 215444![]() |
- | 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 | 215549![]() |
-,- | North African | Hypergammaglobulinaemia,Increased IgA levels | X-linked multisystem autoinflammatory disease with immune dysregulation | PMID:36952639 [Fam.F:II.1(Patient F)] |
104554 | M | 215551![]() |
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 | 215551![]() |
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 | 215551![]() |
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 | 215553![]() |
- | 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 | 215568![]() |
6 | Lebanese | Increased IgA levels | Severe early onset systemic inflammation and autoimmunity | PMID:37349293 [Fam.1:II.1(P1)] |
104678 | F | 215569![]() |
- | Iranian | Increased IgA levels | Severe early onset systemic inflammation and autoimmunity | PMID:37349293 [Fam.2:II.2(P2)] |
105025 | F | 215626![]() |
- | 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 | 215881![]() |
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 | 216001![]() |
3 | Argentinian | Increased IgA levels | Immunodeficiency 117 | PMID:36736301 [Fam.A:II.1(P1)] |
106463 | F | 216023![]() |
- | 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 | 216182![]() |
10 | Caucasian | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:28830446 [P1(II.1)] |
106889 | M | 216182![]() |
4 | Caucasian | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:28830446 [Fam.P1:II.2(P2)] |
106932 | M | 216188![]() |
5 | Jewish | Hypergammaglobulinaemia | Adenosine deaminase 2 deficiency | PMID:25075848 [patient]; PMID:30139808 [Fam.1:II.5(P)] |
107103 | M | 216335![]() |
- | 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 | 216398![]() |
2 | Argentinian | Increased IgA levels | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:35677041 [Pt7]; PMID:29378236 [Fam.1:Patient 1] |
107252 | M | 216399![]() |
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).