ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Infant acute respiratory distress syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	VCP	(0.63)	SFTPC

Citations in the biomedical literature:

Inclusion body myopathy with Paget disease of bone and frontotemporal dementia		Infant acute respiratory distress syndrome
	Synonym(s): - IBMPFD - Limb-girdle muscular dystrophy with Paget disease of bone - Pagetoid amyotrophic lateral sclerosis - Pagetoid neuroskeletal syndrome		Synonym(s): - Hyaline membrane disease - Infant ARDS - Infant respiratory distress syndrome - Neonatal respiratory distress syndrome

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Certain conditions originating in the perinatal period -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: sporadic

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

No signs/symptoms info available.