CUI Disease Vocabulary Name in Vocabulary Code
C1856305 GSD IV, Neuromuscular Form, Childhood DO glycogen storage disease IV 2750
C1856305 GSD IV, Neuromuscular Form, Childhood MONDO glycogen storage disease due to glycogen branching enzyme deficiency 0009292
C1856305 GSD IV, Neuromuscular Form, Childhood MONDO glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form 0017700
C1856305 GSD IV, Neuromuscular Form, Childhood MSH GSD IV, Neuromuscular Form, Childhood C565543
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM GLYCOGEN STORAGE DISEASE IV 232500
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM AMYLOPECTINOSIS 232500
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM GSD IV, CLASSIC HEPATIC 232500
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM GSD IV, NEUROMUSCULAR FORM, FATAL PERINATAL 232500
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM GSD IV, NEUROMUSCULAR FORM, CONGENITAL 232500
C1856305 GSD IV, Neuromuscular Form, Childhood OMIM GSD IV, NEUROMUSCULAR FORM, CHILDHOOD 232500
C1856305 GSD IV, Neuromuscular Form, Childhood ORDO Glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form 308698