Congenital neutropaeniaGene: FCGR3B
Comment when marking as ready: Associated with Neutropenia, alloimmune neonatal on OMIM, no disease association on G2P, two expert reviewers suggest it as red and only found in 1/4 sources
Created: 24 May 2016, 8:14 p.m.
Maternal deficiency of the encoded protein can set the stage for transient neonatal isoimmune thrombocytopenia
Created: 19 Oct 2015, 10:41 p.m.
Model of inheritance for gene FCGR3B was set to Unknown
Phenotypes for gene FCGR3B were set to Neutropenia,alloimmuneneonatal
This gene has been classified as Red List (Low Evidence).
FCGR3B was added to Congenital neutropaeniapanel. Source: Radboud University Medical Center, Nijmegen
FCGR3B was added to Congenital neutropaeniapanel. Sources: Radboud University Medical Center, Nijmegen