Acute monocytic leukemia
Symptom Information:
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) |