congenital neutropenia Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A form of neutropenia with congenital onset. (Human Phenotype Ontology, HP_0005549)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C0340970
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Genes

1 genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
TCIRG1 T-cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 subunit A3