Bone-marrow foam cells

Symptom Information:

Symptom ID: HPO:0004333
Synonyms:
Bone marrow foam cells [HPO:0004333]
Large vacuolated foam cells ('NP cells') on bone marrow biopsy [HPO:0004333]
Large vacuolated foam cells on bone marrow biopsy [HPO:0004333]
Bone marrow foam cells [OMIM:Bone marrow foam cells]
Large vacuolated foam cells ('NP cells') on bone marrow biopsy [OMIM:Large vacuolated foam cells ('NP cells') on bone marrow biopsy]
Bone marrow foam cells (type II) [OMIM:Bone marrow foam cells (type II)]
Quality:
Cross references:
OMIM: "Bone marrow foam cells" [OMIM:Bone marrow foam cells]
OMIM: "Large vacuolated foam cells ('NP cells') on bone marrow biopsy" [OMIM:Large vacuolated foam cells ('NP cells') on bone marrow biopsy]
OMIM: "Bone marrow foam cells (type II)" [OMIM:Bone marrow foam cells (type II)]
Is a (Direct Parents):
HPO         Abnormality of macrophages
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 macrophages(HPO:0004311)
                   Bone-marrow foam cells(HPO:0004333)
       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)
                      Bone-marrow foam cells(HPO:0004333)
MedDRA:
Database Frequency: 11 / 7739
Resource:

All diseases associated with this symptom:

Cholesteryl ester storage disease (Orphanet:75234)
Lysosomal acid lipase deficiency (Orphanet:275761)
NEPHROSIALIDOSIS (OMIM:256150)
NIEMANN-PICK DISEASE, TYPE C1 (OMIM:257220)
NIEMANN-PICK DISEASE, TYPE C2 (OMIM:607625)
Niemann-Pick disease type A (Orphanet:77292)
Niemann-Pick disease type B (Orphanet:77293)
Niemann-Pick disease type E (Orphanet:99022)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Wolman disease (Orphanet:75233)