ODCs

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

PROTEIN INTERACTIONS: 1

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

Autosomal recessive limb-girdle muscular dystrophy type 2J

Lethal congenital contracture syndrome type 3

TTN	(UniProt - OMIM)		MYBPC1	(UniProt - OMIM)
			PIP5K1C	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN	(0.75)	MYBPC1

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2J		Lethal congenital contracture syndrome type 3
	Synonym(s): - LGMD2J		Synonym(s): - LCCS3

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

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

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

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.