Cytopenias and congenital anaemiasGene: FCGR3B
Relevant phenotype affects neutrophils only, on a transient basis owing to presence of antibodies in mother and antigen in fetus (as a result of different genetic factors in father and mother.). Therefore not a germline condition associated with mutations in the child.
Created: 9 Mar 2017, 4:32 p.m.
Mode of inheritance
Other - please specify in evaluation comments
Neutropenia, alloimmune neonatal
Promoted to V1 on 11 March 2017, after internal review and discussion with the clinical team.
FCGR3B was added to Cytopaenias and congenital anaemiaspanel. Source: Expert Review Red Model of inheritance for gene FCGR3B was set to Other - please specify in evaluation comments
FCGR3B was added to Cytopaenias and congenital anaemiaspanel. Sources: Radboud University Medical Center, Nijmegen
FCGR3B was created by LouiseD