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

BRAF FGFR1
FGFR1
KIAA1549
KRAS
NTRK2
RAF1
SRGAP3


COMMON
GENES
FGFR1



Citations in the biomedical literature:


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



Pilocytic astrocytoma
Myeloid neoplasm associated with FGFR1 rearrangement

Synonym(s):
(no synonyms)

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

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

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

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

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

No signs/symptoms info available.