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- NCIT_C148369 IAO_0000115 "An autosomal recessive muscular dystrophy caused by mutation(s) in the LMNA gene, encoding prelamin-A/C. Limb-girdle muscular dystrophy type 1B and Emery-Dreifuss muscular dystrophy-2 are allelic disorders with overlapping phenotypes." @default.
- NCIT_C148369 NCIT_NHC0 "C148369" @default.
- NCIT_C148369 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C148369 NCIT_P108 "Muscular Dystrophy Congenital, LMNA-Related" @default.
- NCIT_C148369 NCIT_P207 "C2750785" @default.
- NCIT_C148369 NCIT_P322 "Cellosaurus" @default.
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- NCIT_C148369 normalizedInformationContent "100" @default.
- NCIT_C148369 referenceCount "1" @default.
- NCIT_C148369 hasExactSynonym "MDCL" @default.
- NCIT_C148369 hasExactSynonym "Muscular Dystrophy Congenital, LMNA-Related" @default.
- NCIT_C148369 inSubset NCIT_C165258 @default.
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- NCIT_C148369 type Class @default.
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- NCIT_C148369 label "Muscular Dystrophy Congenital, LMNA-Related" @default.
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