ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
5 signs/symptoms

Autosomal dominant Emery-Dreifuss muscular dystrophy

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 dominant Emery-Dreifuss muscular dystrophy		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 cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease

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

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

	External references: 4 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 dominant Emery-Dreifuss muscular dystrophy
(no data available)