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Limited systemic sclerosis

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Distal 17p13.3 microdeletion syndrome

1 associated gene
No signs/symptoms info

Limited systemic sclerosis

Distal 17p13.3 microdeletion syndrome

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Limited systemic sclerosis		Distal 17p13.3 microdeletion syndrome
	Synonym(s): - Systemic sclerosis sine scleroderma		Synonym(s): - Distal del(17)(p13.3 ) - Distal monosomy 17p13.3

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

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: - Type of inheritance: sporadic		Epidemiological data: (no data available)

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

No signs/symptoms info available.