ODCs

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

COMMON GENES: 1

1 associated gene
No signs/symptoms info

Scapuloperoneal amyotrophy

Autosomal dominant limb-girdle muscular dystrophy type 1E

DES

DES

Citations in the biomedical literature:

Scapuloperoneal amyotrophy		Autosomal dominant limb-girdle muscular dystrophy type 1E
	Synonym(s): - Kaeser syndrome - Neurogenic scapuloperoneal syndrome - Stark-Kaeser syndrome		Synonym(s): - LGMD1E

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: no data available Type of inheritance: autosomal dominant

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

No signs/symptoms info available.