Bloodwork

ICD-10-CM codes

The diagnosis classification on lab requisitions and clinical records. Every condition on this site is anchored to an ICD-10-CM code.

By chapter

22 chapters

All codes

97,584 codes · page 100 of 1,952

Morquio A mucopolysaccharidoses E76.210 Morquio B mucopolysaccharidoses E76.211 Morquio mucopolysaccharidoses, unspecified E76.219 Sanfilippo mucopolysaccharidoses E76.22 Other mucopolysaccharidoses E76.29 Mucopolysaccharidosis, unspecified E76.3 Other disorders of glucosaminoglycan metabolism E76.8 Glucosaminoglycan metabolism disorder, unspecified E76.9 Disorders of glycoprotein metabolism E77 Defects in post-translational modification of lysosomal enzymes E77.0 Defects in glycoprotein degradation E77.1 Other disorders of glycoprotein metabolism E77.8 Disorder of glycoprotein metabolism, unspecified E77.9 Disorders of lipoprotein metabolism and other lipidemias E78 Pure hypercholesterolemia E78.0 Pure hypercholesterolemia, unspecified E78.00 Familial hypercholesterolemia E78.01 Pure hyperglyceridemia E78.1 Mixed hyperlipidemia E78.2 Hyperchylomicronemia E78.3 Other hyperlipidemia E78.4 Elevated Lipoprotein(a) E78.41 Other hyperlipidemia E78.49 Hyperlipidemia, unspecified E78.5 Lipoprotein deficiency E78.6 Disorders of bile acid and cholesterol metabolism E78.7 Disorder of bile acid and cholesterol metabolism, unspecified E78.70 Barth syndrome E78.71 Smith-Lemli-Opitz syndrome E78.72 Other disorders of bile acid and cholesterol metabolism E78.79 Other disorders of lipoprotein metabolism E78.8 Lipoid dermatoarthritis E78.81 Other lipoprotein metabolism disorders E78.89 Disorder of lipoprotein metabolism, unspecified E78.9 Disorders of purine and pyrimidine metabolism E79 Hyperuricemia w/o signs of inflam arthrit and tophaceous dis Hyperuricemia without signs of inflammatory arthritis and tophaceous disease E79.0 Lesch-Nyhan syndrome E79.1 Myoadenylate deaminase deficiency E79.2 Other disorders of purine and pyrimidine metabolism E79.8 Aicardi-Goutieres syndrome E79.81 Hereditary xanthinuria E79.82 Other specified disorders of purine and pyrimidine metabolism E79.89 Disorder of purine and pyrimidine metabolism, unspecified E79.9 Disorders of porphyrin and bilirubin metabolism E80 Hereditary erythropoietic porphyria E80.0 Porphyria cutanea tarda E80.1 Other and unspecified porphyria E80.2 Unspecified porphyria E80.20 Acute intermittent (hepatic) porphyria E80.21 Other porphyria E80.29