ICD-10-CM codes

97,584 codes · page 100 of 1,952

ICD-10	Description
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
E77	Disorders of glycoprotein metabolism
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
E78	Disorders of lipoprotein metabolism and other lipidemias
E780	Pure hypercholesterolemia
E7800	Pure hypercholesterolemia, unspecified
E7801	Familial hypercholesterolemia
E781	Pure hyperglyceridemia
E782	Mixed hyperlipidemia
E783	Hyperchylomicronemia
E784	Other hyperlipidemia
E7841	Elevated Lipoprotein(a)
E7849	Other hyperlipidemia
E785	Hyperlipidemia, unspecified
E786	Lipoprotein deficiency
E787	Disorders of bile acid and cholesterol metabolism
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
E788	Other disorders of lipoprotein metabolism
E7881	Lipoid dermatoarthritis
E7889	Other lipoprotein metabolism disorders
E789	Disorder of lipoprotein metabolism, unspecified
E79	Disorders of purine and pyrimidine metabolism
E790	Hyperuricemia w/o signs of inflam arthrit and tophaceous dis 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
E7981	Aicardi-Goutieres syndrome
E7982	Hereditary xanthinuria
E7989	Other specified disorders of purine and pyrimidine metabolism
E799	Disorder of purine and pyrimidine metabolism, unspecified
E80	Disorders of porphyrin and bilirubin metabolism
E800	Hereditary erythropoietic porphyria
E801	Porphyria cutanea tarda
E802	Other and unspecified porphyria
E8020	Unspecified porphyria
E8021	Acute intermittent (hepatic) porphyria
E8029	Other porphyria

← prev · next →