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- NCIT_C3213 IAO_0000115 "A rare non-inherited disorder primarily affecting the skin and skeletal system. It is classified as a mesodermal dysplasia. Clinical signs appear within the first decade and are characterized by multiple soft tissue hemiangiomas and enchondromas leading to skeletal deformities. Clinical course is progressive with variable development of associated malignancies." @default.
- NCIT_C3213 NCIT_NHC0 "C3213" @default.
- NCIT_C3213 NCIT_P106 "Disease or Syndrome" @default.
- NCIT_C3213 NCIT_P108 "Maffucci Syndrome" @default.
- NCIT_C3213 NCIT_P207 "C0024454" @default.
- NCIT_C3213 NCIT_P322 "PCDC" @default.
- NCIT_C3213 NCIT_P366 "Maffucci_Syndrome" @default.
- NCIT_C3213 NCIT_R126 NCIT_C107377 @default.
- NCIT_C3213 NCIT_R126 NCIT_C166354 @default.
- NCIT_C3213 NCIT_R126 NCIT_C166356 @default.
- NCIT_C3213 NCIT_R126 NCIT_C26729 @default.
- NCIT_C3213 NCIT_R126 NCIT_C27551 @default.
- NCIT_C3213 NCIT_R126 NCIT_C27574 @default.
- NCIT_C3213 NCIT_R126 NCIT_C2931 @default.
- NCIT_C3213 NCIT_R126 NCIT_C2991 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3007 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3085 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3262 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3263 @default.
- NCIT_C3213 NCIT_R126 NCIT_C35117 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3677 @default.
- NCIT_C3213 NCIT_R126 NCIT_C3810 @default.
- NCIT_C3213 NCIT_R126 NCIT_C4741 @default.
- NCIT_C3213 NCIT_R126 NCIT_C4755 @default.
- NCIT_C3213 NCIT_R126 NCIT_C4784 @default.
- NCIT_C3213 NCIT_R126 NCIT_C4880 @default.
- NCIT_C3213 NCIT_R126 NCIT_C53459 @default.
- NCIT_C3213 NCIT_R126 NCIT_C53684 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7057 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7059 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7062 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7387 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7388 @default.
- NCIT_C3213 NCIT_R126 NCIT_C7389 @default.
- NCIT_C3213 NCIT_R126 NCIT_C8537 @default.
- NCIT_C3213 NCIT_R126 NCIT_C8592 @default.
- NCIT_C3213 NCIT_R126 NCIT_C9343 @default.
- NCIT_C3213 normalizedInformationContent "95.413332725061409" @default.
- NCIT_C3213 referenceCount "2" @default.
- NCIT_C3213 hasExactSynonym "Chondrodysplasia with Hemangioma" @default.
- NCIT_C3213 hasExactSynonym "Chondroplasia Angiomatosis" @default.
- NCIT_C3213 hasExactSynonym "Dyschondroplasia and Cavernous Hemangioma" @default.
- NCIT_C3213 hasExactSynonym "Enchondromatosis with Hemangiomata" @default.
- NCIT_C3213 hasExactSynonym "Hemangiomata with Dyschondroplasia" @default.
- NCIT_C3213 hasExactSynonym "Maffucci Syndrome" @default.
- NCIT_C3213 hasExactSynonym "Maffucci's Anomalad" @default.
- NCIT_C3213 inSubset NCIT_C179478 @default.
- NCIT_C3213 inSubset NCIT_C179491 @default.
- NCIT_C3213 type Class @default.
- NCIT_C3213 isDefinedBy ncit.owl @default.
- NCIT_C3213 label "Maffucci Syndrome" @default.
- NCIT_C3213 subClassOf NCIT_C28193 @default.
- NCIT_C3213 subClassOf NCIT_C2991 @default.
- NCIT_C3213 subClassOf NCIT_C3213 @default.
- NCIT_C3213 subClassOf NCIT_C35561 @default.
- NCIT_C3213 subClassOf NCIT_C4873 @default.
- NCIT_C3213 subClassOf NCIT_C54705 @default.
- NCIT_C3213 subClassOf NCIT_C7057 @default.
- NCIT_C3213 equivalentClass B127fe9851e4dd0fe0f0948a75532e9d1 @default.
- NCIT_C3213 equivalentClass B273b97394d930d5fc4dca3b61c02e43d @default.