Abnormality of macrophages

Symptom Information:

Symptom ID: HPO:0004311
Synonyms:
Abnormality of histiocytes [HPO:0004311]
Macrophages anomaly [Orphanet:48560]
Monocytes/macrophages anomalies [Orphanet:48560]
Monocytes anomaly [Orphanet:48560]
Quality:
Cross references:
Orphanet:48560 "Monocytes/macrophages anomalies" [Orphanet:48560]
Is a (Direct Parents):
Orphanet Abnormality of leukocytes
HPO         Abnormal macrophage count
HPO         Abnormality of myeloid leukocytes
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 macrophages(HPO:0004311)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Abnormality of myeloid leukocytes(HPO:0010974)
                Abnormality of macrophages(HPO:0004311)
MedDRA:
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

Ataxia - pancytopenia (Orphanet:2585)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Glycogen storage disease due to glucose-6-phosphatase deficiency type b (Orphanet:79259)
Hairy cell leukemia variant (Orphanet:300878)
Neutropenia - monocytopenia - deafness (Orphanet:2690)
[DEL] GLYCOGEN STORAGE DISEASE Ib (OMIM:232220)
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 (OMIM:612541)