ODCs

Cytoscape Web

Click node...

Craniopharyngioma

2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Marfan syndrome type 2

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

Craniopharyngioma

Marfan syndrome type 2

BRAF	(UniProt - OMIM)		TGFBR2	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.73)	TGFBR2

Citations in the biomedical literature:

Craniopharyngioma		Marfan syndrome type 2
	Synonym(s): (no synonyms)		Synonym(s): - Loeys-Dietz syndrome type 2 - MFS2

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare circulatory system disease - Rare genetic disease - Rare surgical thoracic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	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: - Average age onset: variable Average age of death: any age Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D003397		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.