Monocytosis
Symptom Information:
Symptom ID: | HPO:0012311 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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 monocyte/macrophage lineage(HPO:0012144) Abnormal monocyte count(HPO:0012310) Monocytosis(HPO:0012311) MedDRA: Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of leukocytes(HPO:0001881) Leukocytoses NEC(MedDRA:10024379) Monocytosis(HPO:0012311) |
||||
Database Frequency: | 10 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Autosomal dominant severe congenital neutropenia | (Orphanet:486) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Barth syndrome | (Orphanet:111) |
Cyclic neutropenia | (Orphanet:2686) |
HOLOPROSENCEPHALY, RECURRENT INFECTIONS, AND MONOCYTOSIS | (OMIM:610680) |
Kostmann syndrome | (Orphanet:99749) |
NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT | (OMIM:613107) |
Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER | (OMIM:614470) |