Showing codes E756 (Lipid storage disorder, unspecified) — E804 (Gilbert syndrome)
ICD-10 Code: E756 (E75.6)
Code Type: Diagnosis
Description:
Lipid storage disorder, unspecified
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ICD-10 Code: E76 (E76)
Code Type: Diagnosis
Description:
Disorders of glycosaminoglycan metabolism
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ICD-10 Code: E760 (E76.0)
Code Type: Diagnosis
Description:
Mucopolysaccharidosis, type I
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ICD-10 Code: E7601 (E76.01)
Code Type: Diagnosis
Description:
Hurler's syndrome
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ICD-10 Code: E7602 (E76.02)
Code Type: Diagnosis
Description:
Hurler-Scheie syndrome
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ICD-10 Code: E7603 (E76.03)
Code Type: Diagnosis
Description:
Scheie's syndrome
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ICD-10 Code: E761 (E76.1)
Code Type: Diagnosis
Description:
Mucopolysaccharidosis, type II
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ICD-10 Code: E762 (E76.2)
Code Type: Diagnosis
Description:
Other mucopolysaccharidoses
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ICD-10 Code: E7621 (E76.21)
Code Type: Diagnosis
Description:
Morquio mucopolysaccharidoses
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ICD-10 Code: E76210 (E76.210)
Code Type: Diagnosis
Description:
Morquio A mucopolysaccharidoses
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ICD-10 Code: E76211 (E76.211)
Code Type: Diagnosis
Description:
Morquio B mucopolysaccharidoses
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ICD-10 Code: E76219 (E76.219)
Code Type: Diagnosis
Description:
Morquio mucopolysaccharidoses, unspecified
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ICD-10 Code: E7622 (E76.22)
Code Type: Diagnosis
Description:
Sanfilippo mucopolysaccharidoses
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ICD-10 Code: E7629 (E76.29)
Code Type: Diagnosis
Description:
Other mucopolysaccharidoses
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ICD-10 Code: E763 (E76.3)
Code Type: Diagnosis
Description:
Mucopolysaccharidosis, unspecified
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ICD-10 Code: E768 (E76.8)
Code Type: Diagnosis
Description:
Other disorders of glucosaminoglycan metabolism
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ICD-10 Code: E769 (E76.9)
Code Type: Diagnosis
Description:
Glucosaminoglycan metabolism disorder, unspecified
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ICD-10 Code: E77 (E77)
Code Type: Diagnosis
Description:
Disorders of glycoprotein metabolism
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ICD-10 Code: E770 (E77.0)
Code Type: Diagnosis
Description:
Defects in post-translational mod of lysosomal enzymes (Defects in post-translational modification of lysosomal enzymes)
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ICD-10 Code: E771 (E77.1)
Code Type: Diagnosis
Description:
Defects in glycoprotein degradation
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ICD-10 Code: E778 (E77.8)
Code Type: Diagnosis
Description:
Other disorders of glycoprotein metabolism
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ICD-10 Code: E779 (E77.9)
Code Type: Diagnosis
Description:
Disorder of glycoprotein metabolism, unspecified
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ICD-10 Code: E78 (E78)
Code Type: Diagnosis
Description:
Disorders of lipoprotein metabolism and other lipidemias
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ICD-10 Code: E780 (E78.0)
Code Type: Diagnosis
Description:
Pure hypercholesterolemia
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ICD-10 Code: E7800 (E78.00)
Code Type: Diagnosis
Description:
Pure hypercholesterolemia, unspecified
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ICD-10 Code: E7801 (E78.01)
Code Type: Diagnosis
Description:
Familial hypercholesterolemia
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ICD-10 Code: E781 (E78.1)
Code Type: Diagnosis
Description:
Pure hyperglyceridemia
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ICD-10 Code: E782 (E78.2)
Code Type: Diagnosis
Description:
Mixed hyperlipidemia
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ICD-10 Code: E783 (E78.3)
Code Type: Diagnosis
Description:
Hyperchylomicronemia
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ICD-10 Code: E784 (E78.4)
Code Type: Diagnosis
Description:
Other hyperlipidemia
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ICD-10 Code: E7841 (E78.41)
Code Type: Diagnosis
Description:
Elevated Lipoprotein(a)
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ICD-10 Code: E7849 (E78.49)
Code Type: Diagnosis
Description:
Other hyperlipidemia
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ICD-10 Code: E785 (E78.5)
Code Type: Diagnosis
Description:
Hyperlipidemia, unspecified
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ICD-10 Code: E786 (E78.6)
Code Type: Diagnosis
Description:
Lipoprotein deficiency
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ICD-10 Code: E787 (E78.7)
Code Type: Diagnosis
Description:
Disorders of bile acid and cholesterol metabolism
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ICD-10 Code: E7870 (E78.70)
Code Type: Diagnosis
Description:
Disorder of bile acid and cholesterol metabolism, unsp (Disorder of bile acid and cholesterol metabolism, unspecified)
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ICD-10 Code: E7871 (E78.71)
Code Type: Diagnosis
Description:
Barth syndrome
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ICD-10 Code: E7872 (E78.72)
Code Type: Diagnosis
Description:
Smith-Lemli-Opitz syndrome
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ICD-10 Code: E7879 (E78.79)
Code Type: Diagnosis
Description:
Other disorders of bile acid and cholesterol metabolism
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ICD-10 Code: E788 (E78.8)
Code Type: Diagnosis
Description:
Other disorders of lipoprotein metabolism
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ICD-10 Code: E7881 (E78.81)
Code Type: Diagnosis
Description:
Lipoid dermatoarthritis
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ICD-10 Code: E7889 (E78.89)
Code Type: Diagnosis
Description:
Other lipoprotein metabolism disorders
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ICD-10 Code: E789 (E78.9)
Code Type: Diagnosis
Description:
Disorder of lipoprotein metabolism, unspecified
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ICD-10 Code: E79 (E79)
Code Type: Diagnosis
Description:
Disorders of purine and pyrimidine metabolism
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ICD-10 Code: E790 (E79.0)
Code Type: Diagnosis
Description:
Hyperuricemia w/o signs of inflam arthrit and tophaceous dis (Hyperuricemia without signs of inflammatory arthritis and tophaceous disease)
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ICD-10 Code: E791 (E79.1)
Code Type: Diagnosis
Description:
Lesch-Nyhan syndrome
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ICD-10 Code: E792 (E79.2)
Code Type: Diagnosis
Description:
Myoadenylate deaminase deficiency
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ICD-10 Code: E798 (E79.8)
Code Type: Diagnosis
Description:
Other disorders of purine and pyrimidine metabolism
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ICD-10 Code: E7981 (E79.81)
Code Type: Diagnosis
Description:
Aicardi-Goutieres syndrome
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ICD-10 Code: E7982 (E79.82)
Code Type: Diagnosis
Description:
Hereditary xanthinuria
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ICD-10 Code: E7989 (E79.89)
Code Type: Diagnosis
Description:
Oth disrd of purine and pyrimidine metabolism (Other specified disorders of purine and pyrimidine metabolism)
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ICD-10 Code: E799 (E79.9)
Code Type: Diagnosis
Description:
Disorder of purine and pyrimidine metabolism, unspecified
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ICD-10 Code: E80 (E80)
Code Type: Diagnosis
Description:
Disorders of porphyrin and bilirubin metabolism
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ICD-10 Code: E800 (E80.0)
Code Type: Diagnosis
Description:
Hereditary erythropoietic porphyria
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ICD-10 Code: E801 (E80.1)
Code Type: Diagnosis
Description:
Porphyria cutanea tarda
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ICD-10 Code: E802 (E80.2)
Code Type: Diagnosis
Description:
Other and unspecified porphyria
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ICD-10 Code: E8020 (E80.20)
Code Type: Diagnosis
Description:
Unspecified porphyria
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ICD-10 Code: E8021 (E80.21)
Code Type: Diagnosis
Description:
Acute intermittent (hepatic) porphyria
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ICD-10 Code: E8029 (E80.29)
Code Type: Diagnosis
Description:
Other porphyria
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ICD-10 Code: E803 (E80.3)
Code Type: Diagnosis
Description:
Defects of catalase and peroxidase
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ICD-10 Code: E804 (E80.4)
Code Type: Diagnosis
Description:
Gilbert syndrome
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