Hemophagocytosis
Symptom Information:
Symptom ID: | HPO:0012156 | ||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Hemophagocytosis(HPO:0012156) 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) MedDRA: |
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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) |