Granulocytopenia

Symptom Information:

Symptom ID: HPO:0001913
Synonyms:
Granulocytopenia [OMIM:Granulocytopenia]
Granulocytopenia [MedDRA:10018687]
Quality:
Cross references:
OMIM: "Granulocytopenia" [OMIM:Granulocytopenia]
UMLS:C0001824 "Granulocytopenia" [HPO:0001913]
Is a (Direct Parents):
MedDRA Neutropenia
HPO         Abnormality of granulocytes
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Abnormality of myeloid leukocytes(HPO:0010974)
                   Abnormality of granulocytes(HPO:0001911)
                      Granulocytopenia(HPO:0001913)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of myeloid leukocytes(HPO:0010974)
                Abnormality of granulocytes(HPO:0001911)
                   Granulocytopenia(HPO:0001913)
MedDRA:
Blood and lymphatic system disorders(MedDRA:10005329)
    Abnormality of leukocytes(HPO:0001881)
       Neutropenia(HPO:0001875)
          Granulocytopenia(HPO:0001913)
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       White blood cell analyses(MedDRA:10047938)
          Neutropenia(HPO:0001875)
             Granulocytopenia(HPO:0001913)
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Barth syndrome (Orphanet:111)
GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY (OMIM:233600)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3 (OMIM:608898)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Reticular dysgenesis (Orphanet:33355)