Congenital agranulocytosis

Symptom Information:

Symptom ID: HPO:0005541
Synonyms:
Congenital agranulocytosis [OMIM:Congenital agranulocytosis]
Quality:
Cross references:
OMIM: "Congenital agranulocytosis" [OMIM:Congenital agranulocytosis]
Is a (Direct Parents):
HPO         Agranulocytosis
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)
                         Agranulocytosis(HPO:0012234)
                            Congenital agranulocytosis(HPO:0005541)
       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)
                      Agranulocytosis(HPO:0012234)
                         Congenital agranulocytosis(HPO:0005541)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant severe congenital neutropenia (Orphanet:486)
Reticular dysgenesis (Orphanet:33355)