Search Ontology:
Human Disease

myofibrillar myopathy 3

Term ID
DOID:0080094
Synonyms
  • autosomal dominant limb-girdle muscular dystrophy type 1A
  • LGMD 1A
  • myotilinopathy
  • spheroid body myopathy
Definition
A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the MYOT gene on chromosome 5q31. (4)
References
Ontology
Human Disease   ( DOID:0080094 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Citations
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