RGD Annotation Report for severe congenital neutropenia 7Rat Genome Database

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An association has been curated linking CV627823 and severe congenital neutropenia 7 in Homo sapiens.

The association was inferred by association of genotype and phenotype (IAGP)
The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
1 RGD objects have been annotated to severe congenital neutropenia 7 (DOID:0112129)
0 papers in RGD have been used to annotate CV627823
Curation Notes: ClinVar Annotator: match by term: Neutropenia, severe congenital, 7, autosomal recessive
Original References(s): PMID:28492532

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.