Code
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7
| Description
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228
|
|---|---|
E75249 | Niemann-Pick disease, unspecified |
E7525 | Metachromatic leukodystrophy |
E7526 | Sulfatase deficiency |
E7529 | Other sphingolipidosis |
E753 | Sphingolipidosis, unspecified |
E754 | Neuronal ceroid lipofuscinosis |
E755 | Other lipid storage disorders |
E756 | Lipid storage disorder, unspecified |
E7601 | Hurler's syndrome |
E7602 | Hurler-Scheie syndrome |
E7603 | Scheie's syndrome |
E761 | Mucopolysaccharidosis, type II |
E76210 | Morquio A mucopolysaccharidoses |
E76211 | Morquio B mucopolysaccharidoses |
E76219 | Morquio mucopolysaccharidoses, unspecified |
E7622 | Sanfilippo mucopolysaccharidoses |
E7629 | Other mucopolysaccharidoses |
E763 | Mucopolysaccharidosis, unspecified |
E768 | Other disorders of glucosaminoglycan metabolism |
E769 | Glucosaminoglycan metabolism disorder, unspecified |
E770 | Defects in post-translational modification of lysosomal enzymes |
E771 | Defects in glycoprotein degradation |
E778 | Other disorders of glycoprotein metabolism |
E779 | Disorder of glycoprotein metabolism, unspecified |
E7800 | Pure hypercholesterolemia, unspecified |
E7801 | Familial hypercholesterolemia |
E781 | Pure hyperglyceridemia |
E782 | Mixed hyperlipidemia |
E783 | Hyperchylomicronemia |
E7841 | Elevated Lipoprotein(a) |
E7849 | Other hyperlipidemia |
E785 | Hyperlipidemia, unspecified |
E786 | Lipoprotein deficiency |
E7870 | Disorder of bile acid and cholesterol metabolism, unspecified |
E7871 | Barth syndrome |
E7872 | Smith-Lemli-Opitz syndrome |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
E790 | Hyperuricemia without signs of inflammatory arthritis and tophaceous disease |
E791 | Lesch-Nyhan syndrome |
E792 | Myoadenylate deaminase deficiency |
E798 | Other disorders of purine and pyrimidine metabolism |
E799 | Disorder of purine and pyrimidine metabolism, unspecified |
E800 | Hereditary erythropoietic porphyria |
E801 | Porphyria cutanea tarda |
E8020 | Unspecified porphyria |
E8021 | Acute intermittent (hepatic) porphyria |
E8029 | Other porphyria |
E803 | Defects of catalase and peroxidase |
E804 | Gilbert syndrome |
E805 | Crigler-Najjar syndrome |
E806 | Other disorders of bilirubin metabolism |
E807 | Disorder of bilirubin metabolism, unspecified |
E8300 | Disorder of copper metabolism, unspecified |
E8301 | Wilson's disease |
E8309 | Other disorders of copper metabolism |
E8310 | Disorder of iron metabolism, unspecified |
E83110 | Hereditary hemochromatosis |
E83111 | Hemochromatosis due to repeated red blood cell transfusions |
E83118 | Other hemochromatosis |
E83119 | Hemochromatosis, unspecified |
E8319 | Other disorders of iron metabolism |
E832 | Disorders of zinc metabolism |
E8330 | Disorder of phosphorus metabolism, unspecified |
E8331 | Familial hypophosphatemia |
E8332 | Hereditary vitamin D-dependent rickets (type 1) (type 2) |
E8339 | Other disorders of phosphorus metabolism |
E8340 | Disorders of magnesium metabolism, unspecified |
E8341 | Hypermagnesemia |
E8342 | Hypomagnesemia |
E8349 | Other disorders of magnesium metabolism |
E8350 | Unspecified disorder of calcium metabolism |
E8351 | Hypocalcemia |
E8352 | Hypercalcemia |
E8359 | Other disorders of calcium metabolism |
E8381 | Hungry bone syndrome |
E8389 | Other disorders of mineral metabolism |
E839 | Disorder of mineral metabolism, unspecified |
E840 | Cystic fibrosis with pulmonary manifestations |
E8411 | Meconium ileus in cystic fibrosis |
E8419 | Cystic fibrosis with other intestinal manifestations |
E848 | Cystic fibrosis with other manifestations |
E849 | Cystic fibrosis, unspecified |
E850 | Non-neuropathic heredofamilial amyloidosis |
E851 | Neuropathic heredofamilial amyloidosis |
E852 | Heredofamilial amyloidosis, unspecified |
E853 | Secondary systemic amyloidosis |
E854 | Organ-limited amyloidosis |
E8581 | Light chain (AL) amyloidosis |
E8582 | Wild-type transthyretin-related (ATTR) amyloidosis |
E8589 | Other amyloidosis |
E859 | Amyloidosis, unspecified |
E860 | Dehydration |
E861 | Hypovolemia |
E869 | Volume depletion, unspecified |
E870 | Hyperosmolality and hypernatremia |
E871 | Hypo-osmolality and hyponatremia |
E872 | Acidosis |
Subsets and Splits