ODCs

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

PROTEIN INTERACTIONS: 1

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

Lethal congenital contracture syndrome type 3

X-linked Emery-Dreifuss muscular dystrophy

MYBPC1	(UniProt - OMIM)		EMD	(UniProt - OMIM)
PIP5K1C	(UniProt - OMIM)		FHL1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MYBPC1	(0.84)	FHL1

Citations in the biomedical literature:

Lethal congenital contracture syndrome type 3		X-linked Emery-Dreifuss muscular dystrophy
	Synonym(s): - LCCS3		Synonym(s): - EDMD1

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

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

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: x-linked recessive

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

No signs/symptoms info available.