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- NCIT_C174217 IAO_0000115 "An autosomal dominant condition caused by mutation(s) in the LMNA gene, encoding prelamin-A/C. It is characterized by dilated cardiomyopathy and hypergonadotropic hypogonadism." @default.
- NCIT_C174217 NCIT_NHC0 "C174217" @default.
- NCIT_C174217 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C174217 NCIT_P108 "Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome" @default.
- NCIT_C174217 NCIT_P207 "C0796083" @default.
- NCIT_C174217 NCIT_P322 "Cellosaurus" @default.
- NCIT_C174217 NCIT_R176 NCIT_C16612 @default.
- NCIT_C174217 NCIT_R176 NCIT_C20744 @default.
- NCIT_C174217 NCIT_R176 NCIT_C20745 @default.
- NCIT_C174217 NCIT_R176 NCIT_C30073 @default.
- NCIT_C174217 NCIT_R176 NCIT_C61148 @default.
- NCIT_C174217 normalizedInformationContent "100" @default.
- NCIT_C174217 referenceCount "1" @default.
- NCIT_C174217 hasExactSynonym "DCM-HH" @default.
- NCIT_C174217 hasExactSynonym "Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome" @default.
- NCIT_C174217 hasExactSynonym "Malouf Syndrome" @default.
- NCIT_C174217 hasExactSynonym "Najjar Syndrome" @default.
- NCIT_C174217 inSubset NCIT_C165258 @default.
- NCIT_C174217 inSubset NCIT_C192842 @default.
- NCIT_C174217 type Class @default.
- NCIT_C174217 isDefinedBy ncit.owl @default.
- NCIT_C174217 label "Dilated Cardiomyopathy-Hypergonadotropic Hypogonadism Syndrome" @default.
- NCIT_C174217 subClassOf B18f98fd411ae646ef0904583c63d8054 @default.
- NCIT_C174217 subClassOf B9a4a9843ddfc6b3329ac7aa1c1d3af9b @default.
- NCIT_C174217 subClassOf NCIT_C174217 @default.
- NCIT_C174217 subClassOf NCIT_C28193 @default.
- NCIT_C174217 subClassOf NCIT_C2991 @default.
- NCIT_C174217 subClassOf NCIT_C7057 @default.