ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Autosomal recessive myogenic arthrogryposis multiplex congenita

Gardner syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SYNE1	(0.63)	APC

Citations in the biomedical literature:

Autosomal recessive myogenic arthrogryposis multiplex congenita		Gardner syndrome
	Synonym(s): - Autosomal recessive myogenic AMC - SYNE1-related AMC - SYNE1-related arthrogryposis multiplex congenita		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare eye disease - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease - Rare skin disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Neoplasms -

	Epidemiological data: (no data available)		Epidemiological data: (no data available)

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D005736

No signs/symptoms info available.