Histiocytosis

Symptom Information:

Symptom ID: HPO:0100727
Synonyms:
Histiocytosis [Orphanet:51120]
Histiocytic infiltrate (morphologic abnormality) [Orphanet:51120]
Histiocytosis (morphologic abnormality) [Orphanet:51120]
Histiocystosis [Orphanet:51120]
Histiocytosis [MedDRA:10020117]
Quality:
Cross references:
Orphanet:51120 "Histiocystosis" [Orphanet:51120]
UMLS:C0019618 "Histiocytosis" [Orphanet:51120]
Is a (Direct Parents):
MedDRA Histiocytoses
HPO         Abnormality of macrophages
Orphanet Haematological malignancy
HPO         Mucinous histiocytosis
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)
                      Histiocytosis(HPO:0100727)
       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)
                   Histiocytosis(HPO:0100727)
MedDRA:
Neoplasms benign, malignant and unspecified (incl cysts and polyps)(MedDRA:10029104)
    Haematopoietic neoplasms (excl leukaemias and lymphomas)(MedDRA:10018865)
       Histiocytoses(MedDRA:10020118)
          Histiocytosis(HPO:0100727)
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

Gaucher disease type 2 (Orphanet:77260)
HISTIOCYTOSIS, FAMILIAL LIPOCHROME (OMIM:235900)