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- NCIT_C172637 IAO_0000115 "A rare, low-grade skin neoplasm of mesenchymal cells of unknown lineage with prominent cytoplasmic granularity. The lesions are most commonly non-ulcerated papules or nodules. Most cases are indolent, despite worrisome histopathologic features. Few cases with regional lymph node metastasis have been reported. (WHO 2018)" @default.
- NCIT_C172637 NCIT_NHC0 "C172637" @default.
- NCIT_C172637 NCIT_P106 "Neoplastic Process" @default.
- NCIT_C172637 NCIT_P108 "Primitive Non-Neural Granular Cell Tumor" @default.
- NCIT_C172637 NCIT_P208 "CL978773" @default.
- NCIT_C172637 NCIT_P363 "Uncertain Malignant Potential" @default.
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- NCIT_C172637 normalizedInformationContent "100" @default.
- NCIT_C172637 referenceCount "1" @default.
- NCIT_C172637 hasExactSynonym "Dermal Non-Neural Granular Cell Tumor" @default.
- NCIT_C172637 hasExactSynonym "Non-Neural Granular Cell Tumor" @default.
- NCIT_C172637 hasExactSynonym "PNNGCT" @default.
- NCIT_C172637 hasExactSynonym "Primitive Non-Neural Granular Cell Tumor" @default.
- NCIT_C172637 hasExactSynonym "Primitive Polypoid Granular Cell Tumor" @default.
- NCIT_C172637 type Class @default.
- NCIT_C172637 isDefinedBy ncit.owl @default.
- NCIT_C172637 label "Primitive Non-Neural Granular Cell Tumor" @default.
- NCIT_C172637 subClassOf NCIT_C169100 @default.
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