The association between CLPB (ClpB Family Mitochondrial Disaggregase) and Neutropenia, Severe Congenital, 9, Autosomal Dominant is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.
Sources4
Clinical variants13
Symptoms15
Compounds0
Trials0
Publications1
01
At a glance
Association overview
A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.