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Autosomal recessive limb-girdle muscular dystrophy type 2D
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
1 associated gene
No signs/symptoms info
Autosomal recessive limb-girdle muscular dystrophy type 2D
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

SGCA
(UniProt - OMIM)
 DAG1
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
SGCA
(0.72)
DAG1


Citations in the biomedical literature:


Autosomal recessive limb-girdle muscular dystrophy type 2D
SGCA
Muscle-eye-brain disease with bilateral multicystic leucodystrophy
DAG1



Autosomal recessive limb-girdle muscular dystrophy type 2D
Muscle-eye-brain disease with bilateral multicystic leucodystrophy

Synonym(s):
- Alpha-sarcoglycanopathy
- LGMD2D
- Limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency
Synonym(s):
- MEB disease with bilateral multicystic leucodystrophy
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- 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: unknown
Average age onset: childhood
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.