Acute myeloid leukemia

Symptom Information:

Symptom ID: HPO:0004808
Synonyms:
Acute myeloblastic leukemia [HPO:0004808]
Acute myelocytic leukemia [HPO:0004808]
Acute myelogenous leukemia [HPO:0004808]
Acute myeloblastic leukemia [OMIM:Acute myeloblastic leukemia]
Acute myelocytic leukemia [OMIM:Acute myelocytic leukemia]
Acute myelogenous leukemia [OMIM:Acute myelogenous leukemia]
Acute myeloid leukemia [OMIM:Acute myeloid leukemia]
Leukemia, acute myeloid [OMIM:Leukemia, acute myeloid]
Quality:
Cross references:
OMIM: "Acute myeloblastic leukemia" [OMIM:Acute myeloblastic leukemia]
OMIM: "Acute myelocytic leukemia" [OMIM:Acute myelocytic leukemia]
OMIM: "Acute myelogenous leukemia" [OMIM:Acute myelogenous leukemia]
OMIM: "Acute myeloid leukemia" [OMIM:Acute myeloid leukemia]
OMIM: "Leukemia, acute myeloid" [OMIM:Leukemia, acute myeloid]
Is a (Direct Parents):
HPO         Acute leukemia
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)
                Leukemia(HPO:0001909)
                   Acute leukemia(HPO:0002488)
                      Acute myeloid leukemia(HPO:0004808)
       Abnormality of blood and blood-forming tissues(HPO:0001871)
          Hematological neoplasm(HPO:0004377)
             Leukemia(HPO:0001909)
                Acute leukemia(HPO:0002488)
                   Acute myeloid leukemia(HPO:0004808)
          Abnormality of leukocytes(HPO:0001881)
             Leukemia(HPO:0001909)
                Acute leukemia(HPO:0002488)
                   Acute myeloid leukemia(HPO:0004808)
       Neoplasm(HPO:0002664)
          Neoplasm by anatomical site(HPO:0011793)
             Hematological neoplasm(HPO:0004377)
                Leukemia(HPO:0001909)
                   Acute leukemia(HPO:0002488)
                      Acute myeloid leukemia(HPO:0004808)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

Acute myeloid leukemia (Orphanet:519)
Adult idiopathic neutropenia (Orphanet:2688)
DOHLE BODIES AND LEUKEMIA (OMIM:223350)
Deafness - lymphedema - leukemia (Orphanet:3226)
Familial platelet syndrome with predisposition to acute myelogenous leukemia (Orphanet:71290)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations (Orphanet:319462)
LEUKEMIA, ACUTE MYELOCYTIC, WITH POLYPOSIS COLI AND COLON CANCER (OMIM:246470)
LYSINE-SPECIFIC METHYLTRANSFERASE 2A (OMIM:159555)
MONOSOMY 7 OF BONE MARROW (OMIM:252270)
MYELODYSPLASIA, IMMUNODEFICIENCY, FACIAL DYSMORPHISM, SHORT STATURE,AND PSYCHOMOTOR DELAY (OMIM:601347)
Neutropenia, severe congenital, 1, autosomal dominant (OMIM:202700)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Shwachman-Diamond syndrome (Orphanet:811)