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Atypical chronic myeloid leukemia
1 associated gene
16 connected diseases
No signs/symptoms info
Disease Type of connection
Chronic neutrophilic leukemia
Hereditary neutrophilia
Autosomal dominant hyper-IgE syndrome
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
Autosomal dominant severe congenital neutropenia
Cyclic neutropenia
FTH1-related iron overload
Severe combined immunodeficiency due to LCK deficiency
Synonym(s):
- Subacute myeloid leukemia
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D054438
Gene symbol UniProt reference OMIM reference
CSF3R Q99062138971
No signs/symptoms info available.