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Autosomal recessive limb-girdle muscular dystrophy type 2F
1 OMIM reference -
1 associated gene
9 connected diseases
No signs/symptoms info
Disease Type of connection
Familial isolated dilated cardiomyopathy
Distal myopathy with posterior leg and anterior hand involvement
Muscle filaminopathy
Alpha-1-antichymotrypsin deficiency
Omenn syndrome
Severe combined immunodeficiency due to adenosine deaminase deficiency
Autosomal recessive limb-girdle muscular dystrophy type 2C
Autosomal recessive limb-girdle muscular dystrophy type 2E
Autosomal recessive limb-girdle muscular dystrophy type 2D
Synonym(s):
- Delta-sarcoglycanopathy
- LGMD2F
- Limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
Class of prevalence: 1-9 / 1 000 000
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
SGCD Q92629601411
No signs/symptoms info available.