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- NCIT_C183526 IAO_0000115 "An autosomal recessive form of combined methylmalonic aciduria and homocystinuria, caused by mutation(s) in the ABCD4 gene, encoding lysosomal cobalamin transporter ABCD4." @default.
- NCIT_C183526 NCIT_NHC0 "C183526" @default.
- NCIT_C183526 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C183526 NCIT_P108 "Methylmalonic Aciduria and Homocystinuria, cblJ Type" @default.
- NCIT_C183526 NCIT_P207 "C3553915" @default.
- NCIT_C183526 NCIT_P322 "Cellosaurus" @default.
- NCIT_C183526 NCIT_R176 NCIT_C158414 @default.
- NCIT_C183526 NCIT_R176 NCIT_C16612 @default.
- NCIT_C183526 NCIT_R176 NCIT_C191877 @default.
- NCIT_C183526 NCIT_R176 NCIT_C21281 @default.
- NCIT_C183526 NCIT_R176 NCIT_C21295 @default.
- NCIT_C183526 NCIT_R176 NCIT_C28533 @default.
- NCIT_C183526 normalizedInformationContent "100" @default.
- NCIT_C183526 referenceCount "1" @default.
- NCIT_C183526 hasExactSynonym "MAHCJ" @default.
- NCIT_C183526 hasExactSynonym "Methylmalonic Aciduria and Homocystinuria, cblJ Type" @default.
- NCIT_C183526 inSubset NCIT_C165258 @default.
- NCIT_C183526 inSubset NCIT_C192842 @default.
- NCIT_C183526 type Class @default.
- NCIT_C183526 isDefinedBy ncit.owl @default.
- NCIT_C183526 label "Methylmalonic Aciduria and Homocystinuria, cblJ Type" @default.
- NCIT_C183526 subClassOf B31304e2f1cd2b153a364077927f42ca2 @default.
- NCIT_C183526 subClassOf B88e769c14230083aa3d751d59425d7bf @default.
- NCIT_C183526 subClassOf NCIT_C183526 @default.
- NCIT_C183526 subClassOf NCIT_C2991 @default.
- NCIT_C183526 subClassOf NCIT_C3235 @default.
- NCIT_C183526 subClassOf NCIT_C34816 @default.
- NCIT_C183526 subClassOf NCIT_C4873 @default.
- NCIT_C183526 subClassOf NCIT_C53529 @default.
- NCIT_C183526 subClassOf NCIT_C53543 @default.
- NCIT_C183526 subClassOf NCIT_C53547 @default.
- NCIT_C183526 subClassOf NCIT_C7057 @default.
- NCIT_C183526 subClassOf NCIT_C98986 @default.