ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
5 signs/symptoms

Autosomal codominant severe lipodystrophic laminopathy

Glycogen storage disease due to muscle glycogen phosphorylase deficiency


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

Citations in the biomedical literature:

Autosomal codominant severe lipodystrophic laminopathy		Glycogen storage disease due to muscle glycogen phosphorylase deficiency
	Synonym(s): (no synonyms)		Synonym(s): - GSD due to muscle glycogen phosphorylase deficiency - GSD type 5 - Glycogen storage disease type 5 - Glycogenosis due to muscle glycogen phosphorylase deficiency - Glycogenosis type 5 - McArdle disease - Myophosphorylase deficiency

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

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: normal Type of inheritance: autosomal recessive

	External references: No OMIM references No MeSH references		External references: 1 OMIM reference - 2 MeSH references: C537276 / D006012

Glycogen storage disease due to muscle glycogen phosphorylase deficiency
	Very frequent - Abnormal muscle biopsy / muscle enzymes / CPK / LDH / aldolase / creatin phosphokinase - Autosomal recessive inheritance Frequent - Myopathy Occasional - Renal failure - Structural anomalies of the cardio-circulatory system
Autosomal codominant severe lipodystrophic laminopathy
(no data available)