RUNX1

runt related transcription factor 1
OMIM: 151385
PanelMode of inheritanceDetails
3 panels
R-numbers: R90
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
601399 Platelet disorder, familial, with associated myeloid malignancy
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Class: familial predisp to leukaemia (typ AD), Quantitative and qualitative platelet disorders with propensity to myeloid malignancy, Familial platelet disorder with propensity to myeloid malignancy, AML, MDS, Thrombocytopenia, No other known cancer risks
R-numbers: R347
Signed-off version 1.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
601399 (OMIM phenotype description ID), 601626 Leukemia, acute myeloid, 601399 Platelet disorder, familial, with associated myeloid malignancy