ODCs

Click node...

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

PROTEIN INTERACTIONS: 3

1 associated gene
No signs/symptoms info

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Autosomal codominant severe lipodystrophic laminopathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP HNRNPA1 HNRNPA2B1	(0.63) (0.49) (0.49)	LMNA LMNA LMNA

Citations in the biomedical literature:

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

	Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 3 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.