MS-DRG 642

Principal Diagnosis - Pdx

• E74.02 Pompe disease
• E74.03 Cori disease
• E74.04 McArdle disease
• E74.05 Lysosome-associated membrane protein 2 [LAMP2] deficiency
• E74.09 Other glycogen storage disease
• E74.20 Disorders of galactose metabolism, unspecified
• E74.21 Galactosemia
• E74.29 Other disorders of galactose metabolism
• E74.4 Disorders of pyruvate metabolism and gluconeogenesis
• E74.810 Glucose transporter protein type 1 deficiency
• E74.818 Other disorders of glucose transport
• E74.819 Disorders of glucose transport, unspecified
• E74.89 Other specified disorders of carbohydrate metabolism
• E74.9 Disorder of carbohydrate metabolism, unspecified
• E75.21 Fabry (-Anderson) disease
• E75.22 Gaucher disease
• E75.240 Niemann-Pick disease type A
• E75.241 Niemann-Pick disease type B
• E75.242 Niemann-Pick disease type C
• E75.243 Niemann-Pick disease type D
• E75.244 Niemann-Pick disease type A/B
• E75.248 Other Niemann-Pick disease
• E75.249 Niemann-Pick disease, unspecified
• E75.3 Sphingolipidosis, unspecified
• E75.5 Other lipid storage disorders
• E75.6 Lipid storage disorder, unspecified
• E76.01 Hurler's syndrome
• E76.02 Hurler-Scheie syndrome
• E76.03 Scheie's syndrome
• E76.1 Mucopolysaccharidosis, type II
• E76.210 Morquio A mucopolysaccharidoses
• E76.211 Morquio B mucopolysaccharidoses
• E76.219 Morquio mucopolysaccharidoses, unspecified
• E76.22 Sanfilippo mucopolysaccharidoses
• E76.29 Other mucopolysaccharidoses
• E76.3 Mucopolysaccharidosis, unspecified
• E76.8 Other disorders of glucosaminoglycan metabolism
• E76.9 Glucosaminoglycan metabolism disorder, unspecified
• E77.0 Defects in post-translational modification of lysosomal enzymes
• E77.1 Defects in glycoprotein degradation
• E77.8 Other disorders of glycoprotein metabolism
• E77.9 Disorder of glycoprotein metabolism, unspecified
• E78.00 Pure hypercholesterolemia, unspecified
• E78.01 Familial hypercholesterolemia
• E78.1 Pure hyperglyceridemia
• E78.2 Mixed hyperlipidemia
• E78.3 Hyperchylomicronemia
• E78.41 Elevated Lipoprotein(a)
• E78.49 Other hyperlipidemia
• E78.5 Hyperlipidemia, unspecified
• E78.6 Lipoprotein deficiency
• E78.70 Disorder of bile acid and cholesterol metabolism, unspecified
• E78.79 Other disorders of bile acid and cholesterol metabolism
• E78.81 Lipoid dermatoarthritis
• E78.89 Other lipoprotein metabolism disorders
• E78.9 Disorder of lipoprotein metabolism, unspecified
• E79.1 Lesch-Nyhan syndrome
• E79.2 Myoadenylate deaminase deficiency
• E79.81 Aicardi-Goutieres syndrome
• E79.82 Hereditary xanthinuria
• E79.89 Other specified disorders of purine and pyrimidine metabolism
• E79.9 Disorder of purine and pyrimidine metabolism, unspecified
• E80.0 Hereditary erythropoietic porphyria
• E80.1 Porphyria cutanea tarda
• E80.20 Unspecified porphyria
• E80.21 Acute intermittent (hepatic) porphyria
• E80.29 Other porphyria
• E80.3 Defects of catalase and peroxidase
• E83.00 Disorder of copper metabolism, unspecified
• E83.01 Wilson's disease
• E83.09 Other disorders of copper metabolism
• E83.10 Disorder of iron metabolism, unspecified
• E83.110 Hereditary hemochromatosis
• E83.111 Hemochromatosis due to repeated red blood cell transfusions
• E83.118 Other hemochromatosis
• E83.119 Hemochromatosis, unspecified
• E83.19 Other disorders of iron metabolism
• E83.30 Disorder of phosphorus metabolism, unspecified
• E83.31 Familial hypophosphatemia
• E83.32 Hereditary vitamin D-dependent rickets (type 1) (type 2)
• E83.39 Other disorders of phosphorus metabolism
• E83.89 Other disorders of mineral metabolism
• E83.9 Disorder of mineral metabolism, unspecified
• E88.01 Alpha-1-antitrypsin deficiency
• E88.1 Lipodystrophy, not elsewhere classified
• E88.2 Lipomatosis, not elsewhere classified
• E88.40 Mitochondrial metabolism disorder, unspecified
• E88.41 MELAS syndrome
• E88.42 MERRF syndrome
• E88.43 Disorders of mitochondrial tRNA synthetases
• E88.49 Other mitochondrial metabolism disorders
• E88.810 Metabolic syndrome
• E88.811 Insulin resistance syndrome, Type A
• E88.818 Other insulin resistance
• E88.819 Insulin resistance, unspecified
• E88.89 Other specified metabolic disorders
• E88.9 Metabolic disorder, unspecified
• E88.A Wasting disease (syndrome) due to underlying condition
• H49.811 Kearns-Sayre syndrome, right eye
• H49.812 Kearns-Sayre syndrome, left eye