ODCs

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2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 2

3 OMIM references -
3 associated genes
No signs/symptoms info

Craniopharyngioma

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CTNNB1 CTNNB1	(0.73) (0.63)	HNRNPA1 HNRNPA2B1

Citations in the biomedical literature:

Craniopharyngioma		Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
	Synonym(s): (no synonyms)		Synonym(s): - IBMPFD - Limb-girdle muscular dystrophy with Paget disease of bone - Pagetoid amyotrophic lateral sclerosis - Pagetoid neuroskeletal syndrome

	Classification (Orphanet): - Rare endocrine disease - Rare neurologic disease - Rare oncologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - 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: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: No OMIM references 1 MeSH reference: D003397		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.