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

COMMON GENES: 1

Limited systemic sclerosis

1 associated gene
No signs/symptoms info

Sarcoidosis

Limited systemic sclerosis

BTNL2	(UniProt - OMIM)		HLA-DRB1	(UniProt - OMIM)
HLA-DRB1	(UniProt - OMIM)


COMMON GENES	HLA-DRB1

Citations in the biomedical literature:

Sarcoidosis		Limited systemic sclerosis
	Synonym(s): - Besnier-Boeck-Schaumann disease - Boeck sarcoid - Boeck's sarcoid		Synonym(s): - Systemic sclerosis sine scleroderma

	Classification (Orphanet): - Rare cardiac disease - Rare endocrine disease - Rare eye disease - Rare neurologic disease - Rare renal disease - Rare respiratory disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare cardiac disease - Rare renal disease - Rare respiratory disease - Rare skin disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: sporadic

	External references: 3 OMIM references - 1 MeSH reference: D012507		External references: No OMIM references No MeSH references

No signs/symptoms info available.