Septicaemia
Basic details
Preferred term: Septicaemia
Alt. terms: Septicemia | sepsis | blood stream infection | Systemic Sepsis | blood poisoning
HPO term: Sepsis
HPO code: HP:0100806
GenIA ID: 172
Last updated on: 2021-12-10 17:55:48
Cross ref. with other ontologies
NCIT: C3364
MESH: D018805
EFO: -
OAE: -
SNOMEDCT: -
ICD10: A41.9
Description
The presence of pathogenic microorganisms in the blood stream causing a rapidly progressing systemic reaction that may lead to shock. Symptoms include fever, chills, tachycardia, and increased respiratory rate. It is a medical emergency that requires urgent medical attention.
Hierarchical classification
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101036 | F | 210182![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.B:II.2(B.II.1)]; PMID:29729943 [Fam.B:II.2(B.II.1 (13))]; PMID:34975878 [Fam.F014:III.2(P014)]; PMID:27418640 [P12(5)]; PMID:37740092 [P01] |
101037 | M | 210182![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.B:II.4(B.II.3)]; PMID:30250467 [B.II.3]; PMID:29729943 [Fam.B:II.4(B.II.3 (15))]; PMID:27418640 [P13(5)] |
101038 | F | 210182![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.B:II.6(B.II.4)]; PMID:30250467 [B.II.4]; PMID:29729943 [Fam.B:II.6(B.II.4 (16))]; PMID:34975878 [Fam.F014:III.6(P015)]; PMID:27418640 [P14(5)] |
101040 | F | 210724![]() |
20 | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.GG:II.1(79)]; PMID:31857261 [Patient 15] |
101043 | M | 210725![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.H:II.2(30)]; PMID:34975878 [Fam.F017:P017] |
101076 | F | 210226 | 11 | German | Septicaemia | PMID:34975878 [Fam.F041:P041] | |
101077 | F | 210211 | 14 | German | Septicaemia | PMID:34975878 [Fam.F043:P043] | |
101082 | F | 211226 | 50 | Septicaemia | Adenosine deaminase 2 deficiency | PMID:34975878 [Fam.F048:P048] | |
101127 | F | 210318 | 50 | German | Septicaemia | PMID:34975878 [Fam.F077:P077] | |
101155 | M | 210235 | - | German | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:30250467 [JJ.II.I]; PMID:29729943 [Fam.JJ:II.1(83)]; PMID:34975878 [Fam.F098:P098] |
101167 | M | 211470![]() |
54 | Septicaemia | NFKB1 insufficiency | PMID:34975878 [Fam.F108:P108]; PMID:33486103 [Fam.1:II.1(patient)]; PMID:150198 [Fam.DT:II.1(510)] | |
101309 | M | 212148 | - | Saudi | Septicaemia | Immunodeficiency, common variable, 8 | PMID:25468195 [Fam.A:II.3(P1)]; PMID:26707784 [P15] |
101386 | F | 212164 | 9 | Pakistani | Septicaemia | Immunodeficiency, common variable, 8 | PMID:22981790 [P1(II.1)]; PMID:26707784 [P11] |
101495 | M | 212458 | 1 | Taiwanese | Septicaemia | Activated p110-delta syndrome 1 | PMID:16984281 [P3(II.1)] |
101597 | M | 212618![]() |
0 | Jewish | Septicaemia | ARPC1B deficiency | PMID:29127144 [Fam.P1:II.10(P2)]; PMID:30254128 [P7]; PMID:35767111 [P6] |
101717 | F | 210260![]() |
- | Caucasian | Septicaemia | 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)] |
101727 | M | 210300![]() |
- | North American | Septicaemia | Immunodeficiency, common variable, 15 | PMID:28782633 [Fam.I:II.1(P1)] |
101740 | M | 210300![]() |
- | North American | Septicaemia | Immunodeficiency, common variable, 15 | PMID:28782633 [Fam.I:III.13(P9)] |
101854 | M | 211650 | - | Septicaemia | PMID:34975878 [Fam.F316:P316] | ||
102175 | M | 210725![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:30250467 [Fam.H:II.1]; PMID:29729943 [Fam.H:II.1(29)] |
102216 | F | 214916![]() |
16 | Belgian | Septicaemia | Severe congenital neutropenia 11 | PMID:32325141 [Patient(II.1)] |
102222 | M | 214917 | 63 | German | Septicaemia | NFKB1 insufficiency | PMID:32278790 [BY.I.1]; PMID:35486341 [P074]; PMID:150198 [Fam.DJ:467]; PMID:36105815 [W295C] |
102260 | F | 214926![]() |
1 | Mexican | Septicaemia | ARPC1B deficiency | PMID:32683750 [Fam.case:II.2(sister)]; PMID:36708766 [Fam.A:II.2(P1)] |
102410 | F | 214947![]() |
4 | South Asian | Septicaemia | Hyper-IgE recurrent infection syndrome 4B | PMID:28747427 [Fam.A:II.3(P1)] |
102772 | M | 214985![]() |
28 | Moroccan | Septicaemia | PMID:29907691 [Fam.A:II.1(P1)] | |
102865 | F | 214996![]() |
- | Italian | Septicaemia | ARPC1B deficiency | Hartnup disease | PMID:35967303 [PtII-1(II.1)]; PMID:35967303 [PtII-1(II.1)] |
102900 | F | 215007![]() |
- | Turkish | Septicaemia | T-cell immunodeficiency, congenital alopecia, and nail dystrophy | PMID:30903456 [Fam.P1:II.2(P2)]; PMID:33464451 [Fam.P12:II.2(P13)]; PMID:37419334 [P13(27)] |
103018 | M | 215085![]() |
15 | Japanese | Septicaemia | Immunodeficiency 35 | PMID:17676033 [Tyk2 Pt]; PMID:17088085 [Patient] |
103113 | M | 215100![]() |
2 | Iranian | Septicaemia | Seizures, cortical blindness, microcephaly syndrome | PMID:36212620 [Patient(II.1)] |
103462 | F | 215132![]() |
- | Moroccan | Septicaemia | ARPC1B deficiency | PMID:35767111 [P4(II.2)] |
103541 | M | 215155![]() |
- | Mexican | Septicaemia | ARPC1B deficiency | PMID:36708766 [Fam.B:II.1(P4)] |
103880 | F | 215269![]() |
3 | Finnish | Septicaemia | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:25038750 [P5]; PMID:25349174 [Fam.1:II.4(Patient 1)] |
103969 | F | 215305![]() |
1 | Pakistani | Septicaemia | Hyper-IgE recurrent infection syndrome 1 | PMID:22751495 [Fam.K35:II.2(P45)] |
104002 | F | 215323![]() |
- | Neonatal sepsis | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:25359994 [P6] | |
104296 | M | 215449![]() |
- | Chinese (China) | Septicaemia | Hyper-IgE recurrent infection syndrome 1 | PMID:21107604 [Case(II.1)] |
104398 | M | 215522![]() |
-,0 | Czech | Neonatal sepsis,Septicaemia | Systemic early-onset autoinflammation, vasculitis and hepatopathy | PMID:36932076 [P3(II.1)] |
104568 | F | 215551![]() |
1 | Pakistani | Septicaemia | 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)] |
104583 | F | 215554![]() |
0 | Arab | Neonatal sepsis | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:30804083 [Patient(III.2)]; PMID:35587511 [Fam.K:II.2(4)]; PMID:38914362 [Fam.D:IV.2(049)] |
104619 | M | 215558![]() |
19 | Dutch | Septicaemia | Immunodeficiency 107 | PMID:35587511 [Fam.A:II.3(5)]; PMID:38914362 [Fam.G:II.3(075)] |
104630 | M | 215560![]() |
- | Septicaemia | X-linked multisystem autoinflammatory disease with immune dysregulation | PMID:37342957 [Fam.C:II.2(P3)] | |
104653 | M | 215564![]() |
10 | Mexican | Septicaemia | Immunodeficiency 107 | PMID:35587511 [Fam.C:III.1(5)]; PMID:38914362 [Fam.I:III.1(089)] |
104685 | F | 215571![]() |
0 | Iranian | Septicaemia | Severe early onset systemic inflammation and autoimmunity | PMID:37382373 [Fam.1:VI.6(VI.5)] |
104713 | M | 215571![]() |
0 | Iranian | Septicaemia | Severe early onset systemic inflammation and autoimmunity | PMID:37382373 [Fam.1:VI.5(VI.4)] |
104787 | M | 215573![]() |
- | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25213377 [Fam.A:I.1(A.I.1)]; PMID:27418640 [P1(4)] | |
104838 | M | 215578![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:25329329 [Fam.F:II.2(F.II.2)]; PMID:29729943 [Fam.F:F.II.1 (24)]; PMID:27418640 [P20(5)]; PMID:34619682 [P.56] |
104845 | F | 215579![]() |
- | European | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.NZ:II.2(II.2)]; PMID:26279205 [Fam.NZ:II.2(II2)]; PMID:29403474 [Fam.NZ (5):II.2(II2)]; PMID:29806948 [Fam.NZ:II.2(II.2)]; PMID:30323807 [Fam.2:II.2(II.2)]; PMID:150198 [Fam.AC:II.2(109)] |
104850 | M | 215584 | 0 | Egyptian | Septicaemia | Omenn syndrome 2 | PMID:30307608 [5] |
104858 | M | 215592 | 1 | Egyptian | Septicaemia | Severe combined immunodeficiency 9B, T-B- | PMID:30307608 [11] |
104867 | F | 215601 | 0 | Egyptian | Septicaemia | Severe combined immunodeficiency 9B, T-B- | PMID:30307608 [19] |
104880 | M | 215607 | - | Egyptian | Neonatal sepsis | Severe combined immunodeficiency 9A, T-B- | PMID:30307608 [26] |
104886 | F | 215613![]() |
- | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.G:III.1(G.III.1 (26))]; PMID:25367873 [Fam.1:III.6(III.6)] |
104953 | F | 215622![]() |
74 | Dutch | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.NA:II.14(II.14)]; PMID:26279205 [Fam.NL1:II.18(16)]; PMID:29403474 [Fam.NL1 (5):II.18(16)]; PMID:11583829 [Fam.1:II.17(II:17)]; PMID:16639407 [Fam.1:II.18(16)]; PMID:150198 [Fam.AA:II.18(020)] |
104956 | F | 215622![]() |
55 | Dutch | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.NA:II.18(II.18)]; PMID:26279205 [Fam.NL1:II.22(19)]; PMID:29403474 [Fam.NL1 (5):II.22(19)]; PMID:11583829 [Fam.1:II.21(II:21)]; PMID:16639407 [Fam.1:II.22(19)]; PMID:150198 [Fam.AA:II.22(024)] |
105088 | M | 215638 | - | Japanese | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:26644313 [II.3(II.3)]; PMID:30250467 [M.II.3]; PMID:29729943 [Fam.M:II.3(M.II.3 (37))]; PMID:27418640 [P21(II.3)]; PMID:35087518 [11.1] |
105103 | F | 215641 | 11 | South Korean | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:26478010 [III.2(III.2)] |
105135 | F | 215649![]() |
0 | Moroccan | Neonatal sepsis | Autoinflammation, panniculitis, and dermatosis syndrome | PMID:38914362 [Fam.M:II.1(107)] |
105179 | F | 215661 | - | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.L:I.2(L.I.2 (34))]; PMID:27102614 [Fam.C:I.2(mother)] |
105209 | M | 215666![]() |
39 | Finnish | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.F1:II.1(II.1)]; PMID:28115215 [Fam.1:II.1(F1.II-1)]; PMID:150198 [Fam.AQ:II.1(171)]; PMID:36356849 [Fam.6:II.1(F6:II:1)]; PMID:36105815 [Fam.H67R:II.1(H67R/1)] |
105221 | M | 215666![]() |
-,0 | Finnish | Neonatal sepsis,Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.F1:IV.2(IV.2)]; PMID:28115215 [Fam.1:IV.1(F1.IV-1)]; PMID:150198 [Fam.AQ:IV.1(183)]; PMID:36356849 [Fam.6:IV.1(F6:IV:1)]; PMID:36105815 [Fam.H67R:IV.1(H67R/8)] |
105232 | M | 215672![]() |
48 | Finnish | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.F3:II.1(II.1)]; PMID:29403474 [Fam.3 (9):II.1(F3.II-1)]; PMID:28115215 [Fam.3:II.1(F3.II-1)]; PMID:150198 [Fam.AS:II.1(196)]; PMID:36356849 [Fam.3:II.1(F3:II:1)]; PMID:36892687 [II:1(II.1)]; PMID:38593810 [Fam.1:II.1(F1.II-1)] |
105238 | M | 215672![]() |
28 | Finnish | Septicaemia | NFKB1 insufficiency | PMID:32278790 [Fam.F3:II.5(II.5)]; PMID:29403474 [Fam.3 (9):II.5(F3.II-5)]; PMID:28115215 [Fam.3:II.5(F3.II-5)]; PMID:150198 [Fam.AS:II.9(204)]; PMID:36356849 [Fam.3:II.9(F3:II:9)]; PMID:36892687 [II:5(II.5)]; PMID:38593810 [Fam.1:II.9(F1.II-5)] |
105241 | M | 215673 | 8 | Kuwaiti | Septicaemia | Immunodeficiency, common variable, 8 | PMID:27760045 [P3(II.1)] |
105256 | F | 210008![]() |
- | German | Septicaemia | PMID:32278790 [Fam.AU:I.2(I.2)]; PMID:150198 [Fam.AM:I.2(153)] | |
105314 | F | 215689 | 70 | European | Septicaemia | NFKB1 insufficiency | PMID:32278790 [F.II.1]; PMID:29477724 [Fam.F:II.1(II:1)]; PMID:150198 [Fam.AZ:265]; PMID:36105815 [V98D] |
105333 | F | 215695 | - | European | Septicaemia | NFKB1 insufficiency | PMID:32278790 [N.II.1]; PMID:29477724 [Fam.N:II.1(II:1)]; PMID:150198 [Fam.BH:286] |
105353 | F | 215715 | - | Turkish | Septicaemia | Immunodeficiency, common variable, 8 | PMID:26686526 [P1] |
105361 | F | 215701![]() |
- | Pakistani | Septicaemia | Immunodeficiency 87 | PMID:31308374 [Fam.A:III.3(P2)] |
105458 | M | 215771![]() |
- | Caucasian | Septicaemia | NFKB1 insufficiency | PMID:32278790 [BO.I.1]; PMID:150198 [Fam.BV:II.5(344)]; PMID:31803180 [Fam.E:II.4(S9)]; PMID:36105815 [Fam.R157P:II.5(S9)]; PMID:34619682 [P.210] |
105533 | M | 215791 | 45 | Portuguese | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29225858 [Patient(I.1)] |
105567 | M | 215808 | - | Turkish | Septicaemia | Immunodeficiency, common variable, 8 | PMID:31026575 [P3]; PMID:31432443 [P12] |
105591 | F | 215821 | - | Caucasian | Septicaemia | Activated p110-delta syndrome 1 | PMID:24610295 [Fam.2:II.1(F2P2)] |
105647 | M | 215832 | - | Septicaemia | Immunodeficiency, common variable, 8 | PMID:34368306 [Patient 3] | |
105740 | U | 215845 | - | Septicaemia | NFKB1 insufficiency | PMID:32278790 [R.I.1]; PMID:150198 [Fam.CI:425] | |
105783 | F | 215876![]() |
- | Caucasian | Septicaemia | NFKB1 insufficiency | PMID:150198 [Fam.DR:III.1(483)]; PMID:32972988 [Fam.1:II.1(Index)] |
105850 | F | 215891![]() |
- | Septicaemia | Autoinflammation, immune dysregulation, and eosinophilia | PMID:33864888 [S066(II.6)] | |
105859 | F | 215894![]() |
54 | British | Septicaemia | Immunodeficiency, common variable, 2 | NFKB1 insufficiency | PMID:150198 [Fam.EA:I.2(551)]; PMID:150198 [Fam.EA:I.2(551)]; PMID:34922003 [Fam.A:I.2(A1)]; PMID:34922003 [Fam.A:I.2(A1)] |
105946 | M | 215913![]() |
10 | Caucasian | Septicaemia | NFKB1 insufficiency | PMID:150198 [Fam.EC:II.1(562)]; PMID:36105815 [Fam.R231C:II.1(R231C/2)]; PMID:35003082 [Fam.1:II.1(P2/S.2)]; PMID:34619682 [P.232] |
105949 | M | 215913![]() |
17 | Caucasian | Septicaemia | NFKB1 insufficiency | PMID:150198 [Fam.EC:II.2(563)]; PMID:36105815 [Fam.R231C:II.2(R231C/3)]; PMID:35003082 [Fam.1:II.2(P3/S.3)]; PMID:34619682 [P.233] |
106090 | M | 215946![]() |
0 | Saudi | Neonatal sepsis | T-cell immunodeficiency with thymic aplasia | PMID:33464451 [P11]; PMID:37419334 [P11(27)]; PMID:31151968 [Fam.1:II.2(Patient)] |
106178 | M | 215974![]() |
- | Finnish | Septicaemia | NFKB1 insufficiency | PMID:150198 [Fam.FL:III.2(672)]; PMID:36356849 [Fam.1:III.2(F1:III:2)]; PMID:38593810 [Fam.2:II.2(F2.II-1)] |
106240 | F | 215977 | - | Caucasian | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:29729943 [Fam.UU:IV.14(UU.IV.12 (120))]; PMID:29305966 [IV.2(IV.2)] |
106320 | M | 215984 | 0 | Neonatal sepsis | NFKB1 insufficiency | PMID:150198 [Fam.EX:608]; PMID:36105815 [L196V] | |
106328 | F | 215987![]() |
28 | Italian | Septicaemia | PMID:150198 [Fam.FR:I.2(731)]; PMID:37600787 [Fam.1:I.2(grandmother)] | |
106348 | M | 215995 | 62 | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:30250467 [CO.I.1(I.1)]; PMID:34111452 [CO.I.1 (173)] | |
106393 | F | 216006![]() |
- | German | Septicaemia | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:36273440 [III.3(III.3)] |
106456 | F | 216020![]() |
13 | Chinese (China) | Septicaemia | NFKB1 insufficiency | PMID:150198 [Fam.FS:II.1(737)]; PMID:37705523 [Fam.1:II.1(index)] |
106482 | F | 216035 | - | Egyptian | Septicaemia | Immunodeficiency, common variable, 8 | PMID:32506362 [P17] |
106750 | F | 216121![]() |
1 | Palestinian | Septicaemia | T-negative/B-positive SCID type 1 | PMID:32921793 [Fam.B:II.1(P1-B)] |
106857 | F | 216173![]() |
0 | Caucasian | Septicaemia | Adenosine deaminase 2 deficiency | PMID:31008556 [Fam.5:II.2(P6)] |
106912 | F | 216186 | 49 | Septicaemia | Immunodeficiency, common variable, 8 | PMID:39289195 [Patient(II.2)] | |
106957 | F | 216198 | - | Septicaemia | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:30092289 [P13] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).