Condition: Hypoproteinemia, Hypercatabolic


rs104894481 in PATL2;B2M gene and Hypoproteinemia, Hypercatabolic PMID 16549777 2006 Familial hypercatabolic hypoproteinemia caused by deficiency of the neonatal Fc receptor, FcRn, due to a mutant beta2-microglobulin gene.