Severe influenza infection
Basic details
Preferred term: Severe influenza infection
Alt. terms: recurrent influenza infection | abnormal influenza infection | unusual influenza infection
HPO term: Severe influenza infection
HPO code: HP:0034249
GenIA ID: 17371
Last updated on: 2025-01-30 17:47:26
Cross ref. with other ontologies
NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: -
Description
An unusually severe infection by an influenza virus.
Hierarchical classification
PARENT terms
TERM
Severe influenza infection
CHILD terms
Reported patients added to GenIA DB
SubjectID | Sex | Fam.ID | Age* | Population | MatchedTerm | Diagnosis | Reference & Pub.codes |
---|---|---|---|---|---|---|---|
101082 | F | 211226 | - | (unusual) Viral infection | Adenosine deaminase 2 deficiency | PMID:34975878 [Fam.F048:P048] | |
101093 | M | 211289 | - | German | (unusual) Viral infection | Immunodeficiency, common variable, 8 | PMID:34975878 [Fam.F059:P059]; PMID:31857261 [Patient 4] |
101115 | F | 210778 | - | Caucasian | (unusual) Viral infection | NFKB1 insufficiency | PMID:34975878 [Fam.F069:P069]; PMID:32278790 [AC.I.1]; PMID:150198 [Fam.CK:427] |
101155 | M | 210235 | - | German | (unusual) Viral infection | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:30250467 [JJ.II.I]; PMID:29729943 [Fam.JJ:II.1(83)]; PMID:34975878 [Fam.F098:P098] |
101160 | F | 211433 | - | (unusual) Viral infection | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:34975878 [Fam.F101:P101] | |
102509 | M | 214948![]() |
- | Irish Traveller | (unusual) Viral infection | Immunodeficiency 54 | PMID:16532402 [Fam.A:IV.12(P3)]; PMID:22354167 [Fam.A:IV.12(P1.3)] |
102719 | F | 214981![]() |
0 | Canadian | (unusual) Viral infection | Autoinflammation, immune dysregulation, and eosinophilia | PMID:28111307 [Fam.1:II.2(Patient)]; PMID:36546480 [Fam.1:II.2(II-2)] |
102729 | M | 214981![]() |
0 | Canadian | (unusual) Viral infection | Autoinflammation, immune dysregulation, and eosinophilia | PMID:28111307 [Fam.1:III.1]; PMID:36546480 [Fam.1:III.1(III-1)] |
102730 | M | 214981![]() |
0 | Canadian | (unusual) Viral infection | Autoinflammation, immune dysregulation, and eosinophilia | PMID:28111307 [Fam.1:III.2]; PMID:36546480 [Fam.1:III.2(III-2)] |
102815 | M | 214994 | - | (unusual) Viral infection | Immunodeficiency 8 | PMID:34913575 [Patient] | |
102962 | F | 215058![]() |
0 | North American | (unusual) Viral infection | T-cell immunodeficiency with thymic aplasia | PMID:31566583 [P1(II.1)]; PMID:37419334 [P1] |
103051 | M | 215095![]() |
1 | Finnish | (unusual) Viral infection | Seizures, cortical blindness, microcephaly syndrome | PMID:33662367 [Fam.F1:II.7(P1)] |
104953 | F | 215622![]() |
74 | Dutch | Severe influenza infection | 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)] |
105045 | M | 215631![]() |
- | Caucasian | Severe influenza infection | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:27379089 [P10] |
105543 | M | 215797 | 40 | Severe influenza infection | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:28983403 [P7] | |
106358 | M | 216000 | 19 | Severe influenza infection | CTLA4 haploinsufficiency with autoimmune infiltration | PMID:31993940 [Patient(II.1)] | |
106367 | F | 216003![]() |
1 | Turkish | Severe influenza infection | Immunodeficiency 117 | PMID:36736301 [Fam.B:II.1(P2)] |
107096 | F | 216332 | - | Japanese | (unusual) Viral infection | Infantile-Onset Multisystem Autoimmune Disease 1 | PMID:33501615 [P3] |
*Age: age reported at the first known time of manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).