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Hereditary neutrophilia
1 OMIM reference -
1 associated gene
16 connected diseases
No signs/symptoms info
Disease Type of connection
Atypical chronic myeloid leukemia
Chronic neutrophilic leukemia
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):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare immune disease
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
CSF3R Q99062138971
No signs/symptoms info available.