E723 | Disorders of lysine and hydroxylysine metabolism |
E724 | Disorders of ornithine metabolism |
E7250 | Disorder of glycine metabolism, unspecified |
E7251 | Non-ketotic hyperglycinemia |
E7252 | Trimethylaminuria |
E7253 | Primary hyperoxaluria |
E7259 | Other disorders of glycine metabolism |
E7281 | Disorders of gamma aminobutyric acid metabolism |
E7289 | Other specified disorders of amino-acid metabolism |
E729 | Disorder of amino-acid metabolism, unspecified |
E7400 | Glycogen storage disease, unspecified |
E7401 | von Gierke disease |
E7402 | Pompe disease |
E7403 | Cori disease |
E7404 | McArdle disease |
E7409 | Other glycogen storage disease |
E7420 | Disorders of galactose metabolism, unspecified |
E7421 | Galactosemia |
E7429 | Other disorders of galactose metabolism |
E744 | Disorders of pyruvate metabolism and gluconeogenesis |
E74810 | Glucose transporter protein type 1 deficiency |
E74818 | Other disorders of glucose transport |
E74819 | Disorders of glucose transport, unspecified |
E7489 | Other specified disorders of carbohydrate metabolism |
E749 | Disorder of carbohydrate metabolism, unspecified |
E7521 | Fabry (-Anderson) disease |
E7522 | Gaucher disease |
E75240 | Niemann-Pick disease type A |
E75241 | Niemann-Pick disease type B |
E75242 | Niemann-Pick disease type C |
E75243 | Niemann-Pick disease type D |
E75244 | Niemann-Pick disease type A/B |
E75248 | Other Niemann-Pick disease |
E75249 | Niemann-Pick disease, unspecified |
E753 | Sphingolipidosis, unspecified |
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 |
E7879 | Other disorders of bile acid and cholesterol metabolism |
E7881 | Lipoid dermatoarthritis |
E7889 | Other lipoprotein metabolism disorders |
E789 | Disorder of lipoprotein metabolism, unspecified |
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 |
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 |
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 |
E848 | Cystic fibrosis with other manifestations |
E849 | Cystic fibrosis, unspecified |
E860 | Dehydration |
E861 | Hypovolemia |
E869 | Volume depletion, unspecified |
E870 | Hyperosmolality and hypernatremia |
E871 | Hypo-osmolality and hyponatremia |
E872 | Acidosis |
E873 | Alkalosis |
E874 | Mixed disorder of acid-base balance |
E875 | Hyperkalemia |
E876 | Hypokalemia |
E8770 | Fluid overload, unspecified |
E8771 | Transfusion associated circulatory overload |
E8779 | Other fluid overload |
E878 | Other disorders of electrolyte and fluid balance, not elsewhere classified |
E8801 | Alpha-1-antitrypsin deficiency |
E881 | Lipodystrophy, not elsewhere classified |
E882 | Lipomatosis, not elsewhere classified |
E8840 | Mitochondrial metabolism disorder, unspecified |
E8841 | MELAS syndrome |
E8842 | MERRF syndrome |
E8849 | Other mitochondrial metabolism disorders |
E8881 | Metabolic syndrome |
E8889 | Other specified metabolic disorders |
E889 | Metabolic disorder, unspecified |
E890 | Postprocedural hypothyroidism |
E891 | Postprocedural hypoinsulinemia |
E892 | Postprocedural hypoparathyroidism |
E893 | Postprocedural hypopituitarism |
E895 | Postprocedural testicular hypofunction |
E896 | Postprocedural adrenocortical (-medullary) hypofunction |
H49811 | Kearns-Sayre syndrome, right eye |
H49812 | Kearns-Sayre syndrome, left eye |
H49813 | Kearns-Sayre syndrome, bilateral |
H49819 | Kearns-Sayre syndrome, unspecified eye |
P926 | Failure to thrive in newborn |
Q891 | Congenital malformations of adrenal gland |
Q892 | Congenital malformations of other endocrine glands |
R290 | Tetany |
R620 | Delayed milestone in childhood |
R6250 | Unspecified lack of expected normal physiological development in childhood |
R6251 | Failure to thrive (child) |
R6252 | Short stature (child) |
R6259 | Other lack of expected normal physiological development in childhood |
R627 | Adult failure to thrive |
R630 | Anorexia |
R631 | Polydipsia |
R632 | Polyphagia |
R6330 | Feeding difficulties, unspecified |
R6331 | Pediatric feeding disorder, acute |
R6332 | Pediatric feeding disorder, chronic |
R6339 | Other feeding difficulties |
R634 | Abnormal weight loss |
R635 | Abnormal weight gain |
R636 | Underweight |
R638 | Other symptoms and signs concerning food and fluid intake |
R7301 | Impaired fasting glucose |
R7302 | Impaired glucose tolerance (oral) |
R7303 | Prediabetes |
R7309 | Other abnormal glucose |
R739 | Hyperglycemia, unspecified |
R81 | Glycosuria |
R824 | Acetonuria |
R946 | Abnormal results of thyroid function studies |
R947 | Abnormal results of other endocrine function studies |
S1110XA | Unspecified open wound of thyroid gland, initial encounter |
S1111XA | Laceration without foreign body of thyroid gland, initial encounter |
S1112XA | Laceration with foreign body of thyroid gland, initial encounter |
S1113XA | Puncture wound without foreign body of thyroid gland, initial encounter |
S1114XA | Puncture wound with foreign body of thyroid gland, initial encounter |
S1115XA | Open bite of thyroid gland, initial encounter |
S37812A | Contusion of adrenal gland, initial encounter |
S37813A | Laceration of adrenal gland, initial encounter |
S37818A | Other injury of adrenal gland, initial encounter |
S37819A | Unspecified injury of adrenal gland, initial encounter |
Z6841 | Body mass index [BMI] 40.0-44.9, adult |
Z6842 | Body mass index [BMI] 45.0-49.9, adult |
Z6843 | Body mass index [BMI] 50.0-59.9, adult |
Z6844 | Body mass index [BMI] 60.0-69.9, adult |
Z6845 | Body mass index [BMI] 70 or greater, adult |