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

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 214948tree icon - Irish Traveller (unusual) Viral infection Immunodeficiency 54 PMID:16532402 [Fam.A:IV.12(P3)]; PMID:22354167 [Fam.A:IV.12(P1.3)]
102719 F 214981tree icon 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 214981tree icon 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 214981tree icon 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 215058tree icon 0 North American (unusual) Viral infection T-cell immunodeficiency with thymic aplasia PMID:31566583 [P1(II.1)]; PMID:37419334 [P1]
103051 M 215095tree icon 1 Finnish (unusual) Viral infection Seizures, cortical blindness, microcephaly syndrome PMID:33662367 [Fam.F1:II.7(P1)]
104953 F 215622tree icon 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 215631tree icon - 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 216003tree icon 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).