Congenital agranulocytosis
Symptom Information:
Symptom ID: | HPO:0005541 | ||
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 granulocytes(HPO:0001911) Granulocytopenia(HPO:0001913) Agranulocytosis(HPO:0012234) Congenital agranulocytosis(HPO:0005541) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormality of myeloid leukocytes(HPO:0010974) Abnormality of granulocytes(HPO:0001911) Granulocytopenia(HPO:0001913) Agranulocytosis(HPO:0012234) Congenital agranulocytosis(HPO:0005541) MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant severe congenital neutropenia | (Orphanet:486) |
Reticular dysgenesis | (Orphanet:33355) |