CCAAT/enhancer binding protein alpha
OMIM: 116897
PanelMode of inheritanceDetails
2 panels
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Class: familial predisp to leukaemia (typ AD), Familial AML with mutated CEBPA, AML, No other known cancer risks
R-numbers: R347
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
601626 (OMIM phenotype description ID), 116897 (OMIN gene description ID), 116897 / 601626 Leukemia, acute myeloid, somatic, 601626 Leukemia, acute myeloid, somatic