Other hyperlipidemia Notes: Familial combined hyperlipidemia
E79.8 Other disorders of purine and pyrimidine metabolism Notes: Hereditary xanthinuria
Other disorders of purine and pyrimidine metabolism Notes: Hereditary xanthinuria
E83.00 Disorder of copper metabolism, unspecified
Disorder of copper metabolism, unspecified
E74.09 Other glycogen storage disease Notes: Andersen disease ; Hers disease ; Tauri disease ; Glycogen storage disease, types …
Other glycogen storage disease Notes: Andersen disease ; Hers disease ; Tauri disease ; Glycogen storage disease, types 0, IV, VI-XI ; Liver phosphorylase deficiency ; Muscle phosphofructokinase defic ...
E74.810 Glucose transporter protein type 1 deficiency Notes: De Vivo syndrome ; Glucose transport defect, blood-brain barrier ; …
Glucose transporter protein type 1 deficiency Notes: De Vivo syndrome ; Glucose transport defect, blood-brain barrier ; Glut1 deficiency ; GLUT1 deficiency syndrome 1, infantile onset ; GLUT1 deficien ...
E75.6 Lipid storage disorder, unspecified
Lipid storage disorder, unspecified
E76.9 Glucosaminoglycan metabolism disorder, unspecified
Glucosaminoglycan metabolism disorder, unspecified