Persistent CMV viremia

Basic details

Preferred term: Persistent CMV viremia
Alt. terms:

HPO term: Persistent CMV viremia
HPO code: HP:0032247

GenIA ID: 12545
Last updated on: 2021-08-02 21:50:33

Cross ref. with other ontologies

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

Description

Lasting (uncontrolled) presence of cytomegalovirus in the blood circulation. Note: Persistent CMV infection has important clinical relevance in the global population. Although immune-mediated control of CMV in healthy individuals prevents disease and overt clinical symptoms, immune dysregulation caused by immunosuppressive treatments in transplant and cancer patients, congenital immunodeficiencies, HIV/AIDS, and/or aging can result in CMV viremia, life threatening disease, and even death.

Hierarchical classification

TERM

Persistent CMV viremia

CHILD terms

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101043 M 210725tree icon - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.H:II.2(30)]; PMID:34975878 [Fam.F017:P017]
101479 F 210314tree icon - German Cytomegalovirus infection NFKB1 insufficiency PMID:34975878 [Fam.F160:P160]; PMID:32278790 [Fam.BF:II.2(II.2)]; PMID:29403474 [Fam.(13):II.1(Patient 2)]; PMID:27923702 [Fam.191:II.1(Patient 2)]; PMID:150198 [Fam.AO:II.2(164)]; GRID:001142 [Fam.#:II.2(FR036)]
101553 M 210256 33 German Cytomegalovirus infection Infantile-Onset Multisystem Autoimmune Disease 1 PMID:34975878 [Fam.F182:P182]
101655 F 212630tree icon - Somali Persistent CMV viremia ARPC1B deficiency PMID:30771411 [P5(II.2)]; PMID:35767111 [P3]
101687 F 212635tree icon - Nepalese Persistent CMV viremia ARPC1B deficiency PMID:30771411 [P12(II.1)]
101722 F 210261tree icon - Asian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:25329329 [Fam.D:II.1(D.II.1)]; PMID:29729943 [Fam.D:II.1(D.II.1 (22))]; PMID:27418640 [P18(5)]
101792 M 210991 - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.NN:II.11(NN.II.9(92))]
101799 M 211120 -,- Caucasian Cytomegalovirus infection,Persistent CMV viremia CTLA4 haploinsufficiency with autoimmune infiltration PMID:30250467 [Fam.XX:II.1]; PMID:29729943 [Fam.XX:II.1(126)]
102157 F 214681 - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.R:II.5(45)]
102181 F 214913 3 Cytomegalovirus infection Severe combined immunodeficiency 9A, T-B- PMID:30877075 [Case 22]; PMID:28864286 [P1]; PMID:28769923 [P34]
102262 F 214927tree icon 1 Japanese Cytomegalovirus infection OAS1 immunodeficiency PMID:29455859 [Fam.C:II.1]; PMID:34145065 [P5(II.1)]; PMID:29185156 [P2]
102269 M 214928tree icon 0 Japanese Cytomegalovirus infection OAS1 immunodeficiency PMID:29455859 [Fam.A:II.3]
102901 F 215008tree icon 1 Brasilian Cytomegalovirus infection T-cell immunodeficiency, congenital alopecia, and nail dystrophy PMID:35064468 [patient(II.2)]
102934 F 215035tree icon - Caucasian Cytomegalovirus infection T-cell lymphopenia with or without nail dystrophy, AD PMID:31447097 [P23]; PMID:33464451 [P14(III.1)]; PMID:37419334 [P23(22)]
102935 M 215035tree icon - Caucasian Cytomegalovirus infection T-cell lymphopenia with or without nail dystrophy, AD PMID:31447097 [P24]; PMID:33464451 [Fam.P14:III.2(P15)]; PMID:37419334 [P15(27)]
103076 F 215099tree icon 3 Omani Cytomegalovirus infection Seizures, cortical blindness, microcephaly syndrome PMID:33662367 [Fam.F5:V.5(P6)]
103113 M 215100tree icon - Iranian Cytomegalovirus infection Seizures, cortical blindness, microcephaly syndrome PMID:36212620 [Patient(II.1)]
103462 F 215132tree icon - Moroccan Cytomegalovirus infection ARPC1B deficiency PMID:35767111 [P4(II.2)]
103473 F 215134tree icon 2 French Cytomegalovirus infection Immunodeficiency 55 PMID:28414293 [Fam.A:II.1(P1)]; PMID:14702466 [Fam.1:II.1(P1)]
103478 M 215135tree icon - French Persistent CMV viremia Immunodeficiency 55 PMID:28414293 [Fam.B:II.1(P3)]
104942 F 215622tree icon 53 Dutch Persistent CMV viremia NFKB1 insufficiency PMID:32278790 [Fam.NA:III.18(III.18)]; PMID:26279205 [Fam.NL1:III.19(57)]; PMID:29403474 [Fam.NL1 (5):III.19(57)]; PMID:150198 [Fam.AA:III.19(045)]; PMID:35242131 [Fam.2:I.1(P2)]
105051 F 215634tree icon - Cytomegalovirus infection Infantile-Onset Multisystem Autoimmune Disease 1 PMID:29180260 [Patient(II.1)]
105088 M 215638 - Japanese Cytomegalovirus infection 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]
105316 U 215691 35 European Cytomegalovirus infection NFKB1 insufficiency PMID:32278790 [H.II.1]; PMID:29477724 [Fam.H:II.1(II:1)]; PMID:150198 [Fam.BB:267]
105317 M 215692tree icon 42 European Cytomegalovirus infection NFKB1 insufficiency PMID:32278790 [Fam.J:III.2(III.2)]; PMID:29477724 [Fam.J:III.2(III:2)]; PMID:150198 [Fam.BD:III.2(277)]
105333 F 215695 - European Cytomegalovirus infection NFKB1 insufficiency PMID:32278790 [N.II.1]; PMID:29477724 [Fam.N:II.1(II:1)]; PMID:150198 [Fam.BH:286]
105362 M 215721tree icon 1 Iraqi Cytomegalovirus infection Immunodeficiency 87 PMID:31308374 [Fam.B:II.1(P3)]
105396 F 215733tree icon - Moroccan Cytomegalovirus infection Immunodeficiency 87 PMID:32562707 [Fam.1:II.4(Pt 4)]
105481 M 215777tree icon - Haitian/Hispanic Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:24165795 [Fam.A:II.1(A.1)]
105504 F 215783tree icon - Asian Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:24165795 [Fam.E:II.1(E.1)]
105507 M 215784tree icon - Caucasian Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:24165795 [Fam.D:I.1(D.I.1)]
105509 M 215784tree icon - Caucasian Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:24165795 [Fam.D:II.1(D.II.1)]
105510 F 215784tree icon - Caucasian Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:24165795 [Fam.D:II.2(D.II.2)]
105543 M 215797 - Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:28983403 [P7]
105546 M 215800tree icon - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29867916 [N211(II.1)]; PMID:29729943 [Fam.O:II.1(O.II.1 (42))]
105567 M 215808 - Turkish Cytomegalovirus infection Immunodeficiency, common variable, 8 PMID:31026575 [P3]; PMID:31432443 [P12]
105830 M 215887 4 Polish Cytomegalovirus infection Activated p110-delta syndrome 1 PMID:26437962 [Fam.2 Sporadic pati:2 Sporadic patient 2]
105910 F 215905 51,- Caucasian Cytomegalovirus infection,Persistent CMV viremia CTLA4 haploinsufficiency with autoimmune infiltration PMID:30250467 [K.II.1]; PMID:29729943 [Fam.K:II.1(K.II.1 (33))]
106037 M 215925 - Japanese Persistent CMV viremia CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.DD:II.1(DD.II.1 (75))]; PMID:35087518 [Fam.19:II.1(19.2)]
106047 F 215930 - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.LL:II.1(LL.II.1 (86))]
106094 M 215947 - Caucasian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.VV:II.1(VV.II.1 (124))]
106150 F 215955 - Turkish Cytomegalovirus infection T-cell immunodeficiency, congenital alopecia, and nail dystrophy PMID:33464451 [P10]
106390 M 216005 23 Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:32996901 [Patient(II.1)]
106669 M 216103 - Cytomegalovirus infection NFKB1 insufficiency PMID:150198 [Fam.EE:565]; PMID:35281075 [5]
106750 F 216121tree icon 0,0 Palestinian Cytomegalovirus infection,Persistent CMV viremia T-negative/B-positive SCID type 1 PMID:32921793 [Fam.B:II.1(P1-B)]
106840 M 216167 17 SouthEast Asian Cytomegalovirus infection CTLA4 haploinsufficiency with autoimmune infiltration PMID:35242131 [3]
107103 M 216335tree icon - Chinese (China) Cytomegalovirus infection Infantile-Onset Multisystem Autoimmune Disease 1 PMID:35677041 [Pt1(II.2)]

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