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

Autosomal dominant limb-girdle muscular dystrophy type 1B

BRAF	(UniProt - OMIM)		LMNA	(UniProt - OMIM)
CTNNB1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1	(0.63)	LMNA

Citations in the biomedical literature:

Craniopharyngioma		Autosomal dominant limb-girdle muscular dystrophy type 1B
	Synonym(s): (no synonyms)		Synonym(s): - LGMD1B - Limb-girdle muscular dystrophy due to lamin A/C deficiency

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	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: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - 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.