ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial osteochondritis dissecans

Wagner disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ACAN	(0.78)	VCAN

Citations in the biomedical literature:

Familial osteochondritis dissecans		Wagner disease
	Synonym(s): - Osteochondritis dissecans and short stature		Synonym(s): - Dominant hyaloideoretinal dystrophy of Wagner - VCAN-related vitreoretinopathy - Vitreoretinal degeneration, Wagner type - Wagner syndrome

	Classification (Orphanet): - Rare bone disease - Rare genetic disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Diseases of the eye and adnexa -

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536075

No signs/symptoms info available.