Leukopenia

Symptom Information:

Symptom ID: HPO:0001882
Synonyms:
Leukopenia (disorder) [Orphanet:48400]
Decreased blood leukocyte number (finding) [Orphanet:48400]
Leukopenia [Orphanet:48400]
Leukopenia [OMIM:Leukopenia]
Leukopenia/hypoleukocytosis [Orphanet:48400]
Leukopenia [MedDRA:10024384]
Leucopenia [MedDRA:10024384]
Leukopenia NOS [MedDRA:10024384]
Leukocytopenia [MedDRA:10024384]
Leucocytopenia [MedDRA:10024384]
Leukopenia (less common) [OMIM:Leukopenia (less common)]
Quality:
Cross references:
Orphanet:48400 "Leukopenia/hypoleukocytosis" [Orphanet:48400]
OMIM: "Leukopenia" [OMIM:Leukopenia]
OMIM: "Leukopenia (less common)" [OMIM:Leukopenia (less common)]
UMLS:C0023530 "Leukopenia" [HPO:0001882]
UMLS:C0023530 "Leukopenia" [Orphanet:48400]
Is a (Direct Parents):
HPO         Abnormal leukocyte count
MedDRA Leukopenias NEC
Orphanet Abnormality of leukocytes
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormal leukocyte count(HPO:0011893)
                Leukopenia(HPO:0001882)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormal leukocyte count(HPO:0011893)
                   Leukopenia(HPO:0001882)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of leukocytes(HPO:0001881)
       Leukopenias NEC(MedDRA:10024385)
          Leukopenia(HPO:0001882)
Database Frequency: 51 / 7739
Resource:

All diseases associated with this symptom:

Acute interstitial pneumonia (Orphanet:79126)
Adams-Oliver syndrome (Orphanet:974)
Aggressive systemic mastocytosis (Orphanet:98850)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BONE MARROW FAILURE SYNDROME 2 (OMIM:615715)
Babesiosis (Orphanet:108)
Camurati-Engelmann disease (Orphanet:1328)
Chédiak-Higashi syndrome (Orphanet:167)
Cohen syndrome (Orphanet:193)
Common variable immunodeficiency (Orphanet:1572)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
DIAMOND-BLACKFAN ANEMIA 5 (OMIM:612528)
DK1-CDG (Orphanet:91131)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 2 (OMIM:613989)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
DYSKERATOSIS CONGENITA, AUTOSOMAL RECESSIVE, 5 (OMIM:615190)
Dengue fever (Orphanet:99828)
Ebola hemorrhagic fever (Orphanet:319218)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Fanconi anemia (Orphanet:84)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Ghosal hematodiaphyseal dysplasia (Orphanet:1802)
Griscelli disease (Orphanet:381)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
Hereditary folate malabsorption (Orphanet:90045)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome (Orphanet:363694)
Isovaleric acidemia (Orphanet:33)
Lassa fever (Orphanet:99824)
Leprechaunism (Orphanet:508)
Lysinuric protein intolerance (Orphanet:470)
MYELOLYMPHATIC INSUFFICIENCY (OMIM:310350)
Marburg hemorrhagic fever (Orphanet:99826)
Mixed connective tissue disease (Orphanet:809)
Osteopetrosis (Orphanet:2781)
PANCYTOPENIA AND OCCLUSIVE VASCULAR DISEASE (OMIM:167850)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Recurrent infections-myelofibrosis-nephromegaly syndrome (Orphanet:369852)
Reticular dysgenesis (Orphanet:33355)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
SYSTEMIC LUPUS ERYTHEMATOSUS (OMIM:152700)
Systemic mastocytosis (Orphanet:2467)
Tyrosinemia type 1 (Orphanet:882)
Viral hemorrhagic fever (Orphanet:341)
Vitamin B12-unresponsive methylmalonic acidemia (Orphanet:27)
Vitamin B12-unresponsive methylmalonic acidemia type mut- (Orphanet:79312)
Vitamin B12-unresponsive methylmalonic acidemia type mut0 (Orphanet:289916)