ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal recessive limb-girdle muscular dystrophy type 2T

Laminopathy type Decaudain-Vigouroux


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GMPPB	(0.63)	LMNA

Citations in the biomedical literature:

Autosomal recessive limb-girdle muscular dystrophy type 2T		Laminopathy type Decaudain-Vigouroux
	Synonym(s): - LGMD2T		Synonym(s): - Laminopathy with severe metabolic syndrome and myopathy

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare endocrine disease - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: (no data available)

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

No signs/symptoms info available.