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Autosomal recessive limb-girdle muscular dystrophy type 2M
1 OMIM reference -
1 associated gene
5 connected diseases
No signs/symptoms info
Disease Type of connection
Congenital muscular dystrophy without intellectual disability
Familial isolated dilated cardiomyopathy
Muscle-eye-brain disease
Walker-Warburg syndrome
Proximal myotonic myopathy

Classification (Orphanet):
- Inborn errors of metabolism
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
FKTN O75072607440
No signs/symptoms info available.