Acute monocytic leukemia

Symptom Information:

Symptom ID: HPO:0004845
Synonyms:
Acute monoblastic leukemia [HPO:0004845]
Acute monocytic leukemia [OMIM:Acute monocytic leukemia]
Acute monoblastic leukemia (AML-M5) [OMIM:Acute monoblastic leukemia (AML-M5)]
Quality:
Cross references:
OMIM: "Acute monocytic leukemia" [OMIM:Acute monocytic leukemia]
OMIM: "Acute monoblastic leukemia (AML-M5)" [OMIM:Acute monoblastic leukemia (AML-M5)]
Is a (Direct Parents):
HPO         Acute leukemia
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Abnormality of leukocytes(HPO:0001881)
             Leukemia(HPO:0001909)
                Acute leukemia(HPO:0002488)
                   Acute monocytic leukemia(HPO:0004845)
          Hematological neoplasm(HPO:0004377)
             Leukemia(HPO:0001909)
                Acute leukemia(HPO:0002488)
                   Acute monocytic leukemia(HPO:0004845)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Hematological neoplasm(HPO:0004377)
                Leukemia(HPO:0001909)
                   Acute leukemia(HPO:0002488)
                      Acute monocytic leukemia(HPO:0004845)
       Abnormality of the immune system(HPO:0002715)
          Abnormality of cellular immune system(HPO:0010987)
             Abnormality of leukocytes(HPO:0001881)
                Leukemia(HPO:0001909)
                   Acute leukemia(HPO:0002488)
                      Acute monocytic leukemia(HPO:0004845)
MedDRA:
Database Frequency: 5 / 7739
Resource:

All diseases associated with this symptom:

Autosomal dominant severe congenital neutropenia (Orphanet:486)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
LEUKEMIA, ACUTE MONOCYTIC (OMIM:151380)
LYSINE-SPECIFIC METHYLTRANSFERASE 2A (OMIM:159555)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)