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Pilocytic astrocytoma
7 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
1 OMIM reference -
1 associated gene
No signs/symptoms info
Pilocytic astrocytoma
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency

BRAF
(UniProt - OMIM)
 PHKB
(UniProt - OMIM)
FGFR1
(UniProt - OMIM)
KIAA1549
(UniProt - OMIM)
KRAS
(UniProt - OMIM)
NTRK2
(UniProt - OMIM)
RAF1
(UniProt - OMIM)
SRGAP3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BRAF
(0.72)
PHKB


Citations in the biomedical literature:


Pilocytic astrocytoma
BRAF FGFR1 KIAA1549 KRAS NTRK2 RAF1
SRGAP3
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
PHKB



Pilocytic astrocytoma
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency

Synonym(s):
(no synonyms)

Synonym(s):
- GSD due to liver and muscle phosphorylase kinase deficiency
- GSD type 9B
- GSD type IXb
- Glycogen storage disease type 9B
- Glycogen storage disease type IXb
- Glycogenosis due to liver and muscle phosphorylase kinase deficiency
- Glycogenosis type 9B
- Glycogenosis type IXb
Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
- Rare neurologic disease
Classification (ICD10):
(no data available)
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: -
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal recessive
External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.