ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Craniopharyngioma

Glycogen storage disease due to liver and muscle phosphorylase kinase deficiency

BRAF	(UniProt - OMIM)		PHKB	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)


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

Citations in the biomedical literature:

Craniopharyngioma		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): - Rare endocrine disease - Rare neurologic 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: Class of prevalence: 1-9 / 100 000 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 1 MeSH reference: D003397		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.