Preferred Label : White blood cell count quantitative trait locus 1;
Symbol : WBCQ1;
CISMeF acronym : WBCQ1;
Type : Phenotype, molecular basis known;
Inheritance : Autosomal recessive;
Molecular basis : Caused by mutation in the atypical chemokine receptor 1 gene (ACKR1, 613665.0002);
Prefixed ID : #611862;
Origin ID : 611862;
UMLS CUI : C2676078;
Automatic exact mappings (from CISMeF team)
Genes related to phenotype
Semantic type(s)