Abnormality of leukocytes
Symptom Information:
Symptom ID: | HPO:0001881 | ||||||||||||||||||||||||
Synonyms: |
|
||||||||||||||||||||||||
Quality: | |||||||||||||||||||||||||
Cross references: |
|
||||||||||||||||||||||||
Is a (Direct Parents): | |||||||||||||||||||||||||
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 blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of leukocytes(HPO:0001881) |
||||||||||||||||||||||||
Database Frequency: | 6 / 7739 | ||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
Hoyeraal-Hreidarsson syndrome | (Orphanet:3322) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
WT limb-blood syndrome | (Orphanet:3466) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |