Monocytosis

Symptom Information:

Symptom ID: HPO:0012311
Synonyms:
Monocytosis [OMIM:Monocytosis]
Monocytosis [MedDRA:10027906]
Quality:
Cross references:
OMIM: "Monocytosis" [OMIM:Monocytosis]
Is a (Direct Parents):
HPO         Abnormal monocyte count
MedDRA Leukocytoses NEC
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)