Abnormality of macrophages
Symptom Information:
Symptom ID: | HPO:0004311 | ||||||
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 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: |
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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) |