Congenital neutropenia

Symptom Information:

Symptom ID: HPO:0005549
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         Neutropenia
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)
                      Abnormality of neutrophils(HPO:0001874)
                         Abnormal neutrophil cell number(HPO:0011991)
                            Neutropenia(HPO:0001875)
                               Congenital neutropenia(HPO:0005549)
       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)
                   Abnormality of neutrophils(HPO:0001874)
                      Abnormal neutrophil cell number(HPO:0011991)
                         Neutropenia(HPO:0001875)
                            Congenital neutropenia(HPO:0005549)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Cyclic neutropenia (Orphanet:2686)
Kostmann syndrome (Orphanet:99749)
NEUTROPENIA, LETHAL CONGENITAL, WITH EOSINOPHILIA (OMIM:257100)
NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT (OMIM:613107)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
X-linked severe congenital neutropenia (Orphanet:86788)