Abnormality of myeloid leukocytes

Symptom Information:

Symptom ID: HPO:0010974
Synonyms:
Quality:
Cross references:
Is a (Direct Parents):
HPO         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)
             Abnormality of myeloid leukocytes(HPO:0010974)
       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)
MedDRA:
Database Frequency: 6 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Cyclic neutropenia (Orphanet:2686)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 (OMIM:612541)