OBO ID: DOID:0110280
Term Name: autosomal recessive limb-girdle muscular dystrophy type 2F Search Ontology:
Synonyms:
  • delta-sarcoglycanopathy
  • LGMD2F
  • limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency
Definition: An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the sarcoglycan-delta gene (SGCD). https://www.ncbi.nlm.nih.gov/pubmed/8841194
References:
Ontology: Human Disease   ( DOID:0110280 )
Relationships
is a type of:
OTHER autosomal recessive limb-girdle muscular dystrophy type 2F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SGCD Muscular dystrophy, limb-girdle, autosomal recessive 6 601287
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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