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Hairy cell leukemia
2 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
Hairy cell leukemia
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency

BRAF
(UniProt - OMIM)
 PHKB
(UniProt - OMIM)
IGHV4-34

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


Citations in the biomedical literature:


Hairy cell leukemia
BRAF IGHV4-34
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency
PHKB



Hairy cell leukemia
Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency

Synonym(s):
- HCL
- Leukemic reticuloendotheliosis
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):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Inborn errors of metabolism
- Rare genetic disease
- Rare hepatic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
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
1 MeSH reference: D007943
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.