ODCs

Cytoscape Web

Click node...

Limited systemic sclerosis

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Spastic paraplegia - Paget disease of bone

1 associated gene
No signs/symptoms info

Limited systemic sclerosis

Spastic paraplegia - Paget disease of bone

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HLA-DRB1	(0.63)	VCP

Citations in the biomedical literature:

Limited systemic sclerosis		Spastic paraplegia - Paget disease of bone
	Synonym(s): - Systemic sclerosis sine scleroderma		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare cardiac disease - Rare renal disease - Rare respiratory disease - Rare skin disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): (no data available)

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

	External references: No OMIM references No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.