CUI Disease Vocabulary Name in Vocabulary Code
C0017923 Glycogen Storage Disease Type IV DO glycogen storage disease VII 11721
C0017923 Glycogen Storage Disease Type IV DO glycogen storage disease IV 2750
C0017923 Glycogen Storage Disease Type IV DO glycogen storage disease VI 2754
C0017923 Glycogen Storage Disease Type IV ICD10CM Andersen disease E74.09
C0017923 Glycogen Storage Disease Type IV ICD10CM Hers disease E74.09
C0017923 Glycogen Storage Disease Type IV ICD10CM Liver phosphorylase deficiency E74.09
C0017923 Glycogen Storage Disease Type IV ICD10CM Tauri disease E74.09
C0017923 Glycogen Storage Disease Type IV ICD10CM Muscle phosphofructokinase deficiency E74.09
C0017923 Glycogen Storage Disease Type IV MONDO glycogen storage disease due to glycogen branching enzyme deficiency 0009292
C0017923 Glycogen Storage Disease Type IV MSH Glycogen Storage Disease Type IV D006011
C0017923 Glycogen Storage Disease Type IV NCI Glycogen Storage Disease Type IV C84737
C0017923 Glycogen Storage Disease Type IV OMIM GLYCOGEN STORAGE DISEASE IV 232500
C0017923 Glycogen Storage Disease Type IV OMIM AMYLOPECTINOSIS 232500
C0017923 Glycogen Storage Disease Type IV OMIM GSD IV, CLASSIC HEPATIC 232500
C0017923 Glycogen Storage Disease Type IV OMIM GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL 232500
C0017923 Glycogen Storage Disease Type IV OMIM GSD IV, NEUROMUSCULAR FORM, CONGENITAL 232500
C0017923 Glycogen Storage Disease Type IV OMIM GSD IV, NEUROMUSCULAR FORM, CHILDHOOD 232500
C0017923 Glycogen Storage Disease Type IV ORDO Glycogen storage disease due to glycogen branching enzyme deficiency 367