Hemophagocytosis

Symptom Information:

Symptom ID: HPO:0012156
Synonyms:
Hemophagocytosis (in some patients) [OMIM:Hemophagocytosis (in some patients)]
Quality:
Cross references:
OMIM: "Hemophagocytosis (in some patients)" [OMIM:Hemophagocytosis (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of macrophages
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)
                      Hemophagocytosis(HPO:0012156)
       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)
                   Hemophagocytosis(HPO:0012156)
MedDRA:
Database Frequency: 9 / 7739
Resource:

All diseases associated with this symptom:

Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Gaucher disease type 2 (Orphanet:77260)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 3 (OMIM:608898)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 4 (OMIM:603552)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 5 (OMIM:613101)
LYMPHOPROLIFERATIVE SYNDROME 2 (OMIM:615122)
Lysinuric protein intolerance (Orphanet:470)
X-linked lymphoproliferative disease (Orphanet:2442)