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Autosomal recessive limb-girdle muscular dystrophy type 2C
1 OMIM reference -
1 associated gene
40 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
Atypical Gaucher disease due to saposin C deficiency
Autosomal dominant limb-girdle muscular dystrophy type 1D
Autosomal recessive centronuclear myopathy
Autosomal recessive limb-girdle muscular dystrophy type 2B
Autosomal recessive limb-girdle muscular dystrophy type 2J
Congenital myopathy, Paradas type
Digitotalar dysmorphism
Distal myopathy with anterior tibial onset
Early-onset myopathy with fatal cardiomyopathy
Encephalopathy due to prosaposin deficiency
Familial isolated arrhythmogenic ventricular dysplasia, biventricular form
Familial isolated arrhythmogenic ventricular dysplasia, left dominant form
Familial isolated arrhythmogenic ventricular dysplasia, right dominant form
Glycogen storage disease due to muscle beta-enolase deficiency
Glycogen storage disease due to muscle glycogen phosphorylase deficiency
Hereditary proximal myopathy with early respiratory failure
Infantile Krabbe disease
Lethal congenital contracture syndrome type 3
Metachromatic leukodystrophy, adult form
Metachromatic leukodystrophy, juvenile form
Metachromatic leukodystrophy, late infantile form
Miyoshi myopathy
Tibial muscular dystrophy
Autosomal recessive limb-girdle muscular dystrophy type 2E
Autosomal recessive limb-girdle muscular dystrophy type 2F
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Metachondromatosis
Noonan syndrome
Synonym(s):
- Gamma-sarcoglycanopathy
- LGMD2C
- Limb-girdle muscular dystrophy due to gamma-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
SGCG Q13326608896
No signs/symptoms info available.