Leukopenia

Basic details

Preferred term: Leukopenia
Alt. terms: Decreased white blood cell count | Low white blood cell count | Decreased blood leukocyte number

HPO term: Leukopenia
HPO code: HP:0001882

GenIA ID: 52
Last updated on: 2021-12-10 17:55:48

Cross ref. with other ontologies

NCIT: -
MESH: -
EFO: -
OAE: -
SNOMEDCT: -
ICD10: D72.819

Description

An abnormal decreased number of leukocytes in the blood.

Hierarchical classification

TERM

Leukopenia

CHILD terms

Reported patients added to GenIA DB

SubjectID Sex Fam.ID Age* Population MatchedTerm Diagnosis Reference & Pub.codes
101025 M 210937 59 Leukopenia PMID:34975878 [Fam.F010:P010]
101038 F 210182tree icon - Caucasian Leukopenia 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)]
101045 M 210205tree icon 19 Caucasian Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:25329329 [Fam.A:III.13(A.III.3)]; PMID:29729943 [Fam.A:III.3(9)]; PMID:34975878 [Fam.F018:III.2(P018)]; PMID:27418640 [P11(5)]
101049 F 210205tree icon 22 Caucasian Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:25329329 [Fam.A:III.15(A.III.5)]; PMID:29729943 [Fam.A:III.15(A.III.5 (10))]
101051 F 210205tree icon 30 Caucasian Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:25329329 [Fam.A:III.5(A.III.1)]; PMID:30250467 [A.III.1]; PMID:29729943 [Fam.A:III.5(A.III.1 (8))]; PMID:34975878 [Fam.F018:III.1(P021)]; PMID:27418640 [P10(5)]
101082 F 211226 48 Leukopenia Adenosine deaminase 2 deficiency PMID:34975878 [Fam.F048:P048]
101088 M 211560 44 German Leukopenia PMID:34975878 [Fam.F054:P054]
101091 M 210911 26 Leukopenia DiGeorge syndrome PMID:34975878 [Fam.F057:P057]; PMID:35486341 [P180]
101093 M 211289 50 German Leukopenia Immunodeficiency, common variable, 8 PMID:34975878 [Fam.F059:P059]; PMID:31857261 [Patient 4]
101120 M 210221 41 German Leukopenia PMID:34975878 [Fam.F071:P071]
101129 F 210906 45 German Leukopenia PMID:34975878 [Fam.F078:P078]
101132 M 210304 - German Leukopenia PMID:34975878 [Fam.F081:P081]
101133 M 210896 40 Leukopenia Immunodeficiency, common variable, 13 PMID:34975878 [Fam.F082:P082]
101312 M 212149 7 Lebanese Leukopenia Immunodeficiency, common variable, 8 PMID:25468195 [Fam.B:II.1(P2)]; PMID:26707784 [P16]
101399 F 210189tree icon 16 German Leukopenia Adenosine deaminase 2 deficiency PMID:28493328 [P6]; PMID:26922074 [Fam.Index:II.1(sister1)]
101404 M 210348 19 Leukopenia PMID:34975878 [Fam.F139:P139]
101479 F 210314tree icon - German Leukopenia 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)]
101613 F 210737 13 Leukopenia PMID:34975878 [Fam.F210:P210]
101620 M 211003 11 Leukopenia PMID:34975878 [Fam.F214:P214]
101884 M 212237tree icon - Sudanese Leukopenia Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.A:III.3(A.II.3)]
101913 M 211925 - Leukopenia PMID:34975878 [Fam.F340:P340]
102133 M 214352tree icon - Sudanese Leukopenia Hyper-IgE recurrent infection syndrome 3 PMID:29907690 [Fam.C:II.1(C.II.1)]
102207 M 214915tree icon 61 Leukopenia Tubulointerstitial kidney disease type 5 PMID:27392076 [Fam.2:II.2(II:2)]
102209 F 214915tree icon 27 Leukopenia Tubulointerstitial kidney disease type 5 PMID:27392076 [Fam.2:III.1(III:1)]
102421 M 214949tree icon 15 French Leukopenia Hyper-IgE recurrent infection syndrome 4A PMID:32207811 [Fam.A:III.1(P3)]
102641 M 214973tree icon - European Leukopenia Immunodeficiency 98 with autoinflammation, somatic PMID:33512449 [Fam.5:II.2(P5)]
102786 F 214988tree icon 23 Turkish Leukopenia Hyper-IgE recurrent infection syndrome 3 PMID:29907691 [Fam.D:II.1(P6)]
102803 F 214991tree icon 15 North American Leukopenia Immunodeficiency 8 PMID:25073507 [P1(II.2)]
102814 U 214993tree icon 1 Caucasian Leukopenia SCID with microcephaly, growth retardation, and sensitivity to ionizing radiation PMID:16439205 [Patient]; PMID:12604777 [2BN(II.1)]
102818 M 214993tree icon 4 Caucasian Leukopenia SCID with microcephaly, growth retardation, and sensitivity to ionizing radiation PMID:12604777 [Fam.2BN:II.2(3BN)]
103113 M 215100tree icon 2 Iranian Leukopenia Seizures, cortical blindness, microcephaly syndrome PMID:36212620 [Patient(II.1)]
103281 F 215111tree icon 2 Chinese (China) Leukopenia Immunodeficiency 82 with systemic inflammation PMID:33782605 [Fam.1:II.2(P1)]
103286 M 215112tree icon 2 Ashkenazi Jewish Leukopenia Immunodeficiency 82 with systemic inflammation PMID:33782605 [Fam.2:I.1(P3)]
103834 F 215257tree icon - European Leukopenia Adenosine deaminase 2 deficiency PMID:24552284 [Fam.2:II.3(P2)]
103839 M 215258tree icon - European Leukopenia Adenosine deaminase 2 deficiency PMID:24552284 [Fam.3:II.3(P3)]
103844 F 215259tree icon - European Leukopenia Adenosine deaminase 2 deficiency PMID:24552284 [Fam.4:II.2(P4)]
103848 M 215260tree icon - European Leukopenia Adenosine deaminase 2 deficiency PMID:24552284 [Fam.5:II.1(P5)]
103859 M 215263tree icon - Turkish Leukopenia Adenosine deaminase 2 deficiency PMID:24552284 [Fam.8:II.1(P9)]; PMID:26233953 [Fam.F4:P5]
104307 F 215451tree icon 17 North American Leukopenia Hyper-IgE recurrent infection syndrome 1 PMID:19483664 [Patient(II.1)]; PMID:26292779 [Co2]
105093 F 215639tree icon - Israeli Leukopenia NFKB1 insufficiency PMID:32278790 [Fam.AA:II.2(II.2)]; PMID:29403474 [Patient 2 (8)]; PMID:27365489 [Fam.2:II.2(Pat.2)]; PMID:150198 [Fam.AF:II.2(127)]
105105 F 215643tree icon 15 Caucasian Leukopenia NFKB1 insufficiency PMID:32278790 [Fam.AB:II.1(II.1)]; PMID:29403474 [Fam.(7):II.1(Index)]; PMID:27338827 [Fam.1:II.1(II-1)]; PMID:150198 [Fam.AD:II.1(117)]
105225 F 215671tree icon - Finnish Leukopenia NFKB1 insufficiency PMID:32278790 [Fam.F2:II.2(II.2)]; PMID:29403474 [Fam.2 (9):II.3(F2.II-3)]; PMID:28115215 [Fam.2:II.3(F2.II-3)]; PMID:150198 [Fam.AR:II.3(191)]; PMID:36356849 [Fam.5:II.2(F5:II:2)]
105251 M 215678 - Leukopenia Combined immunodeficiency 36 PMID:33876203 [P1(II.1)]
105363 F 215722 13 Afro-American Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:29729943 [Fam.X:II.1(X.II.1 (59))]; PMID:28366794 [Fam.A:II.1(P1)]
105412 F 215762tree icon 27 Caucasian Leukopenia NFKB1 insufficiency PMID:32278790 [Fam.BB:I.1(I.1)]; PMID:30063981 [Fam.1:II.2(II.2)]; PMID:150198 [Fam.BM:II.3(300)]
105549 F 215801 12 Caucasian Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:29200144 [Fam.A:IV.1(P1)]
105746 M 215851tree icon 57 Finnish Leukopenia Immunodeficiency, common variable, 14 PMID:34451894 [Patient(II.2)]; PMID:37876937 [Fam.C:II.2(C.1)]
105899 F 215900tree icon - North American Leukopenia NFKB1 insufficiency PMID:150198 [Fam.DW:II.1(538)]; PMID:34307247 [Fam.1:II.1(daughter1)]; PMID:28802957 [Fam.1:II.1(II.1)]
106109 M 215952tree icon 4 Iranian Leukopenia NFKB1 insufficiency PMID:150198 [Fam.EG:III.4(584)]; PMID:35392793 [Fam.1:III.4(III-1(index))]
106165 M 215964 - Turkish Leukopenia Immunodeficiency, common variable, 8 PMID:31432443 [P9]
106172 F 215971 - German Leukopenia NFKB1 insufficiency PMID:150198 [Fam.FI:660]; GRID:001142 [FR302]
106223 M 215976tree icon - Finnish Leukopenia NFKB1 insufficiency PMID:150198 [Fam.FN:II.1(710)]; PMID:36356849 [Fam.4:II.1(F4:II:1)]; PMID:38593810 [Fam.3:II.1(F3.II-1)]
106358 M 216000 19 Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:31993940 [Patient(II.1)]
106363 F 216001tree icon 0 Argentinian Leukopenia Immunodeficiency 117 PMID:36736301 [Fam.A:II.1(P1)]
106371 M 216004 17 Leukopenia CTLA4 haploinsufficiency with autoimmune infiltration PMID:29375547 [Fam.A:II.1(A.II.1)]; PMID:31396201 [P2(II.1)]
106423 F 216015tree icon 9 Leukopenia NFKB1 insufficiency PMID:150198 [Fam.FU:III.4(765)]; PMID:38130541 [Fam.1:III.4(P1)]
106760 M 216123tree icon 0 Israeli Leukopenia X-linked severe combined immunodeficiency PMID:32921793 [Fam.A:II.1(P1-A)]
106819 M 216163tree icon 48 Chinese (China) Leukopenia Immunodeficiency, common variable, 1 PMID:36571238 [Fam.2:II.2(II:2[P3])]
106854 F 216173tree icon 1 Caucasian Leukopenia Adenosine deaminase 2 deficiency PMID:31008556 [Fam.5:II.1(P5)]
107225 M 216381tree icon 0 Vietnamese Leukopenia Hemophagocytic lymphohistiocytosis, familial 5 PMID:36503158 [Patient(III.3)]

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