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Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C151898> ?p ?o ?g. }

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NCIT_C151898 IAO_0000115 "Familial acute myeloid leukemia (AML) syndrome associated with biallelic CEBPA mutations. Patients typically present with AML as children or young adults. The familial form of AML with germline CEBPA mutation has morphological and immunophenotypic features similar to those of sporadic AML with CEBPA mutations. Overall, it has a favorable prognosis. (WHO 2017)" @default.
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NCIT_C151898 NCIT_P106 "Neoplastic Process" @default.
NCIT_C151898 NCIT_P108 "Acute Myeloid Leukemia with Germline CEBPA Mutation" @default.
NCIT_C151898 NCIT_P207 "C3711382" @default.
NCIT_C151898 NCIT_P363 "Malignant" @default.
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