Acute myeloid leukemia
Symptom Information:
Symptom ID: | HPO:0004808 | ||||||||
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 leukocytes(HPO:0001881) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) Acute myeloid leukemia(HPO:0004808) Hematological neoplasm(HPO:0004377) Leukemia(HPO:0001909) Acute leukemia(HPO:0002488) Acute myeloid leukemia(HPO:0004808) 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) 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) |