ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

X-linked Emery-Dreifuss muscular dystrophy

Autosomal recessive myogenic arthrogryposis multiplex congenita

EMD	(UniProt - OMIM)		SYNE1	(UniProt - OMIM)
FHL1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EMD	(0.75)	SYNE1

Citations in the biomedical literature:

X-linked Emery-Dreifuss muscular dystrophy		Autosomal recessive myogenic arthrogryposis multiplex congenita
	Synonym(s): - EDMD1		Synonym(s): - Autosomal recessive myogenic AMC - SYNE1-related AMC - SYNE1-related arthrogryposis multiplex congenita

	Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive		Epidemiological data: (no data available)

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.