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ICD-10-CM/PCS MS-DRG v41.0 Definitions Manual

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MDC 10 Endocrine, nutritional and metabolic diseases and disorders
Assignment of Diagnosis Codes
Page 2 of 2
A187 E7204
E7204Cystinosis
E7209Other disorders of amino-acid transport
E7210Disorders of sulfur-bearing amino-acid metabolism, unspecified
E7211Homocystinuria
E7212Methylenetetrahydrofolate reductase deficiency
E7219Other disorders of sulfur-bearing amino-acid metabolism
E7220Disorder of urea cycle metabolism, unspecified
E7221Argininemia
E7222Arginosuccinic aciduria
E7223Citrullinemia
E7229Other disorders of urea cycle metabolism
E723Disorders of lysine and hydroxylysine metabolism
E724Disorders of ornithine metabolism
E7250Disorder of glycine metabolism, unspecified
E7251Non-ketotic hyperglycinemia
E7252Trimethylaminuria
E7253Primary hyperoxaluria
E7259Other disorders of glycine metabolism
E7281Disorders of gamma aminobutyric acid metabolism
E7289Other specified disorders of amino-acid metabolism
E729Disorder of amino-acid metabolism, unspecified
E7400Glycogen storage disease, unspecified
E7401von Gierke disease
E7402Pompe disease
E7403Cori disease
E7404McArdle disease
E7405Lysosome-associated membrane protein 2 [LAMP2] deficiency
E7409Other glycogen storage disease
E7420Disorders of galactose metabolism, unspecified
E7421Galactosemia
E7429Other disorders of galactose metabolism
E744Disorders of pyruvate metabolism and gluconeogenesis
E74810Glucose transporter protein type 1 deficiency
E74818Other disorders of glucose transport
E74819Disorders of glucose transport, unspecified
E7489Other specified disorders of carbohydrate metabolism
E749Disorder of carbohydrate metabolism, unspecified
E7521Fabry (-Anderson) disease
E7522Gaucher disease
E75240Niemann-Pick disease type A
E75241Niemann-Pick disease type B
E75242Niemann-Pick disease type C
E75243Niemann-Pick disease type D
E75244Niemann-Pick disease type A/B
E75248Other Niemann-Pick disease
E75249Niemann-Pick disease, unspecified
E753Sphingolipidosis, unspecified
E755Other lipid storage disorders
E756Lipid storage disorder, unspecified
E7601Hurler's syndrome
E7602Hurler-Scheie syndrome
E7603Scheie's syndrome
E761Mucopolysaccharidosis, type II
E76210Morquio A mucopolysaccharidoses
E76211Morquio B mucopolysaccharidoses
E76219Morquio mucopolysaccharidoses, unspecified
E7622Sanfilippo mucopolysaccharidoses
E7629Other mucopolysaccharidoses
E763Mucopolysaccharidosis, unspecified
E768Other disorders of glucosaminoglycan metabolism
E769Glucosaminoglycan metabolism disorder, unspecified
E770Defects in post-translational modification of lysosomal enzymes
E771Defects in glycoprotein degradation
E778Other disorders of glycoprotein metabolism
E779Disorder of glycoprotein metabolism, unspecified
E7800Pure hypercholesterolemia, unspecified
E7801Familial hypercholesterolemia
E781Pure hyperglyceridemia
E782Mixed hyperlipidemia
E783Hyperchylomicronemia
E7841Elevated Lipoprotein(a)
E7849Other hyperlipidemia
E785Hyperlipidemia, unspecified
E786Lipoprotein deficiency
E7870Disorder of bile acid and cholesterol metabolism, unspecified
E7879Other disorders of bile acid and cholesterol metabolism
E7881Lipoid dermatoarthritis
E7889Other lipoprotein metabolism disorders
E789Disorder of lipoprotein metabolism, unspecified
E791Lesch-Nyhan syndrome
E792Myoadenylate deaminase deficiency
E7981Aicardi-Goutières syndrome
E7982Hereditary xanthinuria
E7989Other specified disorders of purine and pyrimidine metabolism
E799Disorder of purine and pyrimidine metabolism, unspecified
E800Hereditary erythropoietic porphyria
E801Porphyria cutanea tarda
E8020Unspecified porphyria
E8021Acute intermittent (hepatic) porphyria
E8029Other porphyria
E803Defects of catalase and peroxidase
E8300Disorder of copper metabolism, unspecified
E8301Wilson's disease
E8309Other disorders of copper metabolism
E8310Disorder of iron metabolism, unspecified
E83110Hereditary hemochromatosis
E83111Hemochromatosis due to repeated red blood cell transfusions
E83118Other hemochromatosis
E83119Hemochromatosis, unspecified
E8319Other disorders of iron metabolism
E8330Disorder of phosphorus metabolism, unspecified
E8331Familial hypophosphatemia
E8332Hereditary vitamin D-dependent rickets (type 1) (type 2)
E8339Other disorders of phosphorus metabolism
E8340Disorders of magnesium metabolism, unspecified
E8341Hypermagnesemia
E8342Hypomagnesemia
E8349Other disorders of magnesium metabolism
E8350Unspecified disorder of calcium metabolism
E8351Hypocalcemia
E8352Hypercalcemia
E8359Other disorders of calcium metabolism
E8381Hungry bone syndrome
E8389Other disorders of mineral metabolism
E839Disorder of mineral metabolism, unspecified
E848Cystic fibrosis with other manifestations
E849Cystic fibrosis, unspecified
E860Dehydration
E861Hypovolemia
E869Volume depletion, unspecified
E870Hyperosmolality and hypernatremia
E871Hypo-osmolality and hyponatremia
E8720Acidosis, unspecified
E8721Acute metabolic acidosis
E8722Chronic metabolic acidosis
E8729Other acidosis
E873Alkalosis
E874Mixed disorder of acid-base balance
E875Hyperkalemia
E876Hypokalemia
E8770Fluid overload, unspecified
E8771Transfusion associated circulatory overload
E8779Other fluid overload
E878Other disorders of electrolyte and fluid balance, not elsewhere classified
E8801Alpha-1-antitrypsin deficiency
E881Lipodystrophy, not elsewhere classified
E882Lipomatosis, not elsewhere classified
E8840Mitochondrial metabolism disorder, unspecified
E8841MELAS syndrome
E8842MERRF syndrome
E8843Disorders of mitochondrial tRNA synthetases
E8849Other mitochondrial metabolism disorders
E88810Metabolic syndrome
E88811Insulin resistance syndrome, Type A
E88818Other insulin resistance
E88819Insulin resistance, unspecified
E8889Other specified metabolic disorders
E889Metabolic disorder, unspecified
E88AWasting disease (syndrome) due to underlying condition
E890Postprocedural hypothyroidism
E891Postprocedural hypoinsulinemia
E892Postprocedural hypoparathyroidism
E893Postprocedural hypopituitarism
E895Postprocedural testicular hypofunction
E896Postprocedural adrenocortical (-medullary) hypofunction
H49811Kearns-Sayre syndrome, right eye
H49812Kearns-Sayre syndrome, left eye
H49813Kearns-Sayre syndrome, bilateral
H49819Kearns-Sayre syndrome, unspecified eye
P926Failure to thrive in newborn
Q891Congenital malformations of adrenal gland
Q892Congenital malformations of other endocrine glands
R290Tetany
R620Delayed milestone in childhood
R6250Unspecified lack of expected normal physiological development in childhood
R6251Failure to thrive (child)
R6252Short stature (child)
R6259Other lack of expected normal physiological development in childhood
R627Adult failure to thrive
R630Anorexia
R631Polydipsia
R632Polyphagia
R6330Feeding difficulties, unspecified
R6331Pediatric feeding disorder, acute
R6332Pediatric feeding disorder, chronic
R6339Other feeding difficulties
R634Abnormal weight loss
R635Abnormal weight gain
R636Underweight
R638Other symptoms and signs concerning food and fluid intake
R7301Impaired fasting glucose
R7302Impaired glucose tolerance (oral)
R7303Prediabetes
R7309Other abnormal glucose
R739Hyperglycemia, unspecified
R81Glycosuria
R824Acetonuria
R946Abnormal results of thyroid function studies
R947Abnormal results of other endocrine function studies
S1110XAUnspecified open wound of thyroid gland, initial encounter
S1111XALaceration without foreign body of thyroid gland, initial encounter
S1112XALaceration with foreign body of thyroid gland, initial encounter
S1113XAPuncture wound without foreign body of thyroid gland, initial encounter
S1114XAPuncture wound with foreign body of thyroid gland, initial encounter
S1115XAOpen bite of thyroid gland, initial encounter
S37812AContusion of adrenal gland, initial encounter
S37813ALaceration of adrenal gland, initial encounter
S37818AOther injury of adrenal gland, initial encounter
S37819AUnspecified injury of adrenal gland, initial encounter
Z6841Body mass index [BMI] 40.0-44.9, adult
Z6842Body mass index [BMI] 45.0-49.9, adult
Z6843Body mass index [BMI] 50.0-59.9, adult
Z6844Body mass index [BMI] 60.0-69.9, adult
Z6845Body mass index [BMI] 70 or greater, adult



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