Abnormality of cells of the granulocytic lineage
Symptom Information:
Symptom ID: | HPO:0012135 | ||
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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 bone marrow cell morphology(HPO:0005561) Abnormality of cells of the granulocytic lineage(HPO:0012135) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Acute promyelocytic leukemia | (Orphanet:520) |
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia | (Orphanet:363727) |