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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C82596> ?p ?o ?g. }

• NCIT_C82596 IAO_0000115 "A myeloid disorder that occurs in childhood and is characterized by persistent cytopenia, dysplastic changes in at least two hematopoietic lineages or in 10% or more of cells in one hematopoietic lineage, less than 5% blasts in bone marrow, and less than 2% blasts in peripheral blood, absence of bone marrow fibrosis, and absence of history of prior cytotoxic chemotherapy or radiation therapy. In a subset of cases, somatic mutations or cytogenetic abnormalities can be identified. Other cases are the result of pre-existing disorders with germline mutations, including Fanconi anemia, Shwachman-Diamond syndrome, and dyskeratosis congenita." @default.
• NCIT_C82596 NCIT_A32 NCIT_C176985 @default.
• NCIT_C82596 NCIT_A32 NCIT_C177621 @default.
• NCIT_C82596 NCIT_NHC0 "C82596" @default.
• NCIT_C82596 NCIT_P106 "Neoplastic Process" @default.
• NCIT_C82596 NCIT_P108 "Refractory Cytopenia of Childhood" @default.
• NCIT_C82596 NCIT_P207 "C2826323" @default.
• NCIT_C82596 NCIT_P322 "GDC" @default.
• NCIT_C82596 NCIT_P322 "NICHD" @default.
• NCIT_C82596 NCIT_P325 "The most common subtype of the myelodysplastic syndromes affecting children. It is characterized by persistent cytopenia with less than 5% blasts in the bone marrow and less than 2% blasts in the peripheral blood. Most cases are associated with a normal karyotype, however, when abnormal, monosomy 7 is the most frequently seen cytogenetic abnormality." @default.
• NCIT_C82596 NCIT_P334 "9985/3" @default.
• NCIT_C82596 NCIT_P363 "Malignant" @default.
• NCIT_C82596 NCIT_P366 "Refractory_Cytopenia_of_Childhood" @default.
• NCIT_C82596 NCIT_P375 "9985/3" @default.
• NCIT_C82596 NCIT_P375 "Refractory cytopenia of childhood" @default.
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