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

Autosomal recessive limb-girdle muscular dystrophy type 2J

King-Denborough syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TTN	(0.63)	RYR1

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2J		King-Denborough syndrome
	Synonym(s): - LGMD2J		Synonym(s): - Koussef-Nichols syndrome

	Classification (Orphanet): - 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): - Diseases of the nervous system -

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

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536883

No signs/symptoms info available.