has material basis in germline mutation in LDHB glycogen storage disease due to lactate dehydrogenase H-subunit deficiency https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/4985 https://rarediseases.info.nih.gov/diseases/3161/lactate-dehydrogenase-b-deficiency https://www.malacards.org/card/lactate_dehydrogenase_b_deficiency_2 UMLS:C3279904 MONDO:0013587 glycogenosis due to lactate dehydrogenase H-subunit deficiency lactate dehydrogenase deficiency type B LDH-H subunit deficiency MEDGEN:481534 OMIM:614128 lactate dehydrogenase B deficiency GARD:0003161 LDHBD A condition that affects how the body breaks down sugar to use as energy in muscle cells. Unlike people with lactate dehydrogenase A deficiency, people with this condition typically do not have any signs or symptoms. It is unclear why this condition does not cause any health problems. Affected people are usually diagnosed when routine blood tests reveal reduced activity of the enzyme lactate dehydrogenase. LDHBD is caused by mutations in the LDHB gene and is inherited in an autosomal recessive manner. GSD due to lactate dehydrogenase H-subunit deficiency LDH deficiency B Orphanet:284435 lactate dehydrogenase-B deficiency MESH:C563641 glycogen storage disease due to lactate dehydrogenase deficiency disorder of glycolysis