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1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
7 associated genes
No signs/symptoms info
Myeloid neoplasm associated with FGFR1 rearrangement
Pilocytic astrocytoma

FGFR1 BRAF
FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


COMMON
GENES
FGFR1



Citations in the biomedical literature:


Myeloid neoplasm associated with FGFR1 rearrangement
FGFR1
Pilocytic astrocytoma
BRAF KIAA1549 KRAS NTRK2 RAF1
SRGAP3



Myeloid neoplasm associated with FGFR1 rearrangement
Pilocytic astrocytoma

Synonym(s):
- 8p11 myeloproliferative syndrome
- Stem cell leukemia/lymphoma

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
(no data available)
Classification (ICD10):
(no data available)

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references

No signs/symptoms info available.