has material basis in germline mutation in disease has basis in disruption of disease caused by disruption of GK glycerol kinase activity inborn glycerol kinase deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://www.malacards.org/card/glycerol_kinase_deficiency SCTID:124322002 An acquired metabolic disease that has its basis in the disruption of glycerol kinase activity. rare inborn error of glycerol kinase activity inborn error of glycerol kinase activity OMIM:307030 DOID:0060363 Orphanet:308993 inborn glycerol kinase activity disorder UMLS:C0268418 MEDGEN:82803 GARD:0021311 https://github.com/monarch-initiative/mondo/issues/5373 glycerol kinase deficiency, X-linked recessive glycerol kinase deficiency MONDO:0010613 GKD NANDO:2200505 inborn errors of metabolism