Abnormality of phagocytes
Symptom Information:
Symptom ID: | HPO:0010977 | ||
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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 phagocytes(HPO:0010977) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormality of myeloid leukocytes(HPO:0010974) Abnormality of phagocytes(HPO:0010977) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |
[DEL] NEUTROPENIA, SEVERE CONGENITAL, 4, AUTOSOMAL RECESSIVE; SCN4 | (OMIM:612541) |