ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Autosomal dominant limb-girdle muscular dystrophy type 1C

Hyperinsulinism due to INSR deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CAV3	(0.52)	INSR

Citations in the biomedical literature:

Autosomal dominant limb-girdle muscular dystrophy type 1C		Hyperinsulinism due to INSR deficiency
	Synonym(s): - LGMD1C - Limb-girdle muscular dystrophy due to caveolin-3 deficiency		Synonym(s): - Hyperinsulinemic hypoglycemia due to INSR deficiency - Hyperinsulinemic hypoglycemia due to insulin receptor deficiency

	Classification (Orphanet): - 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: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.