{"code":"E71","type":"category","title":"Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["androgen insensitivity syndrome (E34.5-)","congenital adrenal hyperplasia (E25.0)","hemolytic anemias attributable to enzyme disorders (D55.-)","Marfan syndrome (Q87.4-)","5-alpha-reductase deficiency (E29.1)"],"excludes2":["Ehlers-Danlos syndromes (Q79.6-)"],"isBillable":false,"sibling_codes":["E71.0","E71.1","E71.11","E71.110","E71.111","E71.118","E71.12","E71.120","E71.121","E71.128","E71.19","E71.2","E71.3","E71.30","E71.31","E71.310","E71.311","E71.312","E71.313","E71.314","E71.318","E71.32","E71.39","E71.4","E71.40","E71.41","E71.42","E71.43","E71.44","E71.440","E71.448","E71.5","E71.50","E71.51","E71.510","E71.511","E71.518","E71.52","E71.520","E71.521","E71.522","E71.528","E71.529","E71.53","E71.54","E71.540","E71.541","E71.542","E71.548"],"inclusionTerms":[],"sibling_titles":{"code":"E71.548","title":"Other peroxisomal disorders","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"is a non-billable ICD-10-CM category code (E71). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","officialDefinition":"Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism is a non-billable ICD-10-CM category code (E71). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","seventhCharacterInstructions":[],"workflowProtocols":[],"guidelines":{"whenToUse":[],"whenNotToUse":[],"commonBillingMistakes":[],"codeComparisons":[],"documentationChecklist":[]},"domainLandscape":{"summary":"Primary diagnostic domain and clinical landscape evaluation.","keyCategories":[],"diagnosticContinuum":"Progression continuum from acute presentation to resolution."},"children":[{"code":"E71.0","title":"Maple-syrup-urine disease","description":"Maple-syrup-urine disease is a billable ICD-10-CM diagnosis code (E71.0). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.0-maple-syrup-urine-disease"},{"code":"E71.1","title":"Other disorders of branched-chain amino-acid metabolism","description":"Other disorders of branched-chain amino-acid metabolism is a non-billable ICD-10-CM category code (E71.1). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.1-other-disorders-of-branched-chain-amino-acid-metabolism"},{"code":"E71.11","title":"Branched-chain organic acidurias","description":"Branched-chain organic acidurias is a non-billable ICD-10-CM category code (E71.11). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.11-branched-chain-organic-acidurias"},{"code":"E71.110","title":"Isovaleric acidemia","description":"Isovaleric acidemia is a billable ICD-10-CM diagnosis code (E71.110). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.110-isovaleric-acidemia"},{"code":"E71.111","title":"3-methylglutaconic aciduria","description":"3-methylglutaconic aciduria is a billable ICD-10-CM diagnosis code (E71.111). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.111-3-methylglutaconic-aciduria"},{"code":"E71.118","title":"Other branched-chain organic acidurias","description":"Other branched-chain organic acidurias is a billable ICD-10-CM diagnosis code (E71.118). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.118-other-branched-chain-organic-acidurias"},{"code":"E71.12","title":"Disorders of propionate metabolism","description":"Disorders of propionate metabolism is a non-billable ICD-10-CM category code (E71.12). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.12-disorders-of-propionate-metabolism"},{"code":"E71.120","title":"Methylmalonic acidemia","description":"Methylmalonic acidemia is a billable ICD-10-CM diagnosis code (E71.120). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.120-methylmalonic-acidemia"},{"code":"E71.121","title":"Propionic acidemia","description":"Propionic acidemia is a billable ICD-10-CM diagnosis code (E71.121). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.121-propionic-acidemia"},{"code":"E71.128","title":"Other disorders of propionate metabolism","description":"Other disorders of propionate metabolism is a billable ICD-10-CM diagnosis code (E71.128). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.128-other-disorders-of-propionate-metabolism"},{"code":"E71.19","title":"Other disorders of branched-chain amino-acid metabolism","description":"Other disorders of branched-chain amino-acid metabolism is a billable ICD-10-CM diagnosis code (E71.19). Inclusion terms: Hyperleucine-isoleucinemia; Hypervalinemia. Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.19-other-disorders-of-branched-chain-amino-acid-metabolism"},{"code":"E71.2","title":"Disorder of branched-chain amino-acid metabolism, unspecified","description":"Disorder of branched-chain amino-acid metabolism, unspecified is a billable ICD-10-CM diagnosis code (E71.2). Excludes1 (not coded here): androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.2-disorder-of-branched-chain-amino-acid-metabolism-unspecified"},{"code":"E71.3","title":"Disorders of fatty-acid metabolism","description":"Disorders of fatty-acid metabolism is a non-billable ICD-10-CM category code (E71.3). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.3-disorders-of-fatty-acid-metabolism"},{"code":"E71.30","title":"Disorder of fatty-acid metabolism, unspecified","description":"Disorder of fatty-acid metabolism, unspecified is a billable ICD-10-CM diagnosis code (E71.30). Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.30-disorder-of-fatty-acid-metabolism-unspecified"},{"code":"E71.31","title":"Disorders of fatty-acid oxidation","description":"Disorders of fatty-acid oxidation is a non-billable ICD-10-CM category code (E71.31). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.31-disorders-of-fatty-acid-oxidation"},{"code":"E71.310","title":"Long chain/very long chain acyl CoA dehydrogenase deficiency","description":"Long chain/very long chain acyl CoA dehydrogenase deficiency is a billable ICD-10-CM diagnosis code (E71.310). Inclusion terms: LCAD deficiency; VLCAD deficiency. Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.310-long-chainvery-long-chain-acyl-coa-dehydrogenase-deficiency"},{"code":"E71.311","title":"Medium chain acyl CoA dehydrogenase deficiency","description":"Medium chain acyl CoA dehydrogenase deficiency is a billable ICD-10-CM diagnosis code (E71.311). Inclusion terms: MCAD deficiency. Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.311-medium-chain-acyl-coa-dehydrogenase-deficiency"},{"code":"E71.312","title":"Short chain acyl CoA dehydrogenase deficiency","description":"Short chain acyl CoA dehydrogenase deficiency is a billable ICD-10-CM diagnosis code (E71.312). Inclusion terms: SCAD deficiency. Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.312-short-chain-acyl-coa-dehydrogenase-deficiency"},{"code":"E71.313","title":"Glutaric aciduria type II","description":"Glutaric aciduria type II is a billable ICD-10-CM diagnosis code (E71.313). Inclusion terms: Glutaric aciduria type II A; Glutaric aciduria type II B; Glutaric aciduria type II C. Excludes1 (not coded here): glutaric aciduria (type 1) NOS (E72.3); peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.313-glutaric-aciduria-type-ii"},{"code":"E71.314","title":"Muscle carnitine palmitoyltransferase deficiency","description":"Muscle carnitine palmitoyltransferase deficiency is a billable ICD-10-CM diagnosis code (E71.314). Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.314-muscle-carnitine-palmitoyltransferase-deficiency"},{"code":"E71.318","title":"Other disorders of fatty-acid oxidation","description":"Other disorders of fatty-acid oxidation is a billable ICD-10-CM diagnosis code (E71.318). Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.318-other-disorders-of-fatty-acid-oxidation"},{"code":"E71.32","title":"Disorders of ketone metabolism","description":"Disorders of ketone metabolism is a billable ICD-10-CM diagnosis code (E71.32). Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.32-disorders-of-ketone-metabolism"},{"code":"E71.39","title":"Other disorders of fatty-acid metabolism","description":"Other disorders of fatty-acid metabolism is a billable ICD-10-CM diagnosis code (E71.39). Excludes1 (not coded here): peroxisomal disorders (E71.5); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): carnitine deficiency due to inborn error of metabolism (E71.42); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.39-other-disorders-of-fatty-acid-metabolism"},{"code":"E71.4","title":"Disorders of carnitine metabolism","description":"Disorders of carnitine metabolism is a non-billable ICD-10-CM category code (E71.4). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.4-disorders-of-carnitine-metabolism"},{"code":"E71.40","title":"Disorder of carnitine metabolism, unspecified","description":"Disorder of carnitine metabolism, unspecified is a billable ICD-10-CM diagnosis code (E71.40). Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.40-disorder-of-carnitine-metabolism-unspecified"},{"code":"E71.41","title":"Primary carnitine deficiency","description":"Primary carnitine deficiency is a billable ICD-10-CM diagnosis code (E71.41). Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.41-primary-carnitine-deficiency"},{"code":"E71.42","title":"Carnitine deficiency due to inborn errors of metabolism","description":"Carnitine deficiency due to inborn errors of metabolism is a billable ICD-10-CM diagnosis code (E71.42). Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-). Code also: associated inborn error or metabolism.","isBillable":true,"slug":"e71.42-carnitine-deficiency-due-to-inborn-errors-of-metabolism"},{"code":"E71.43","title":"Iatrogenic carnitine deficiency","description":"Iatrogenic carnitine deficiency is a billable ICD-10-CM diagnosis code (E71.43). Inclusion terms: Carnitine deficiency due to hemodialysis; Carnitine deficiency due to Valproic acid therapy. Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.43-iatrogenic-carnitine-deficiency"},{"code":"E71.44","title":"Other secondary carnitine deficiency","description":"Other secondary carnitine deficiency is a non-billable ICD-10-CM category code (E71.44). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.44-other-secondary-carnitine-deficiency"},{"code":"E71.440","title":"Ruvalcaba-Myhre-Smith syndrome","description":"Ruvalcaba-Myhre-Smith syndrome is a billable ICD-10-CM diagnosis code (E71.440). Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.440-ruvalcaba-myhre-smith-syndrome"},{"code":"E71.448","title":"Other secondary carnitine deficiency","description":"Other secondary carnitine deficiency is a billable ICD-10-CM diagnosis code (E71.448). Excludes1 (not coded here): Muscle carnitine palmitoyltransferase deficiency (E71.314); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.448-other-secondary-carnitine-deficiency"},{"code":"E71.5","title":"Peroxisomal disorders","description":"Peroxisomal disorders is a non-billable ICD-10-CM category code (E71.5). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.5-peroxisomal-disorders"},{"code":"E71.50","title":"Peroxisomal disorder, unspecified","description":"Peroxisomal disorder, unspecified is a billable ICD-10-CM diagnosis code (E71.50). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.50-peroxisomal-disorder-unspecified"},{"code":"E71.51","title":"Disorders of peroxisome biogenesis","description":"Disorders of peroxisome biogenesis is a non-billable ICD-10-CM category code (E71.51). A more specific billable subcode must be selected for claims submission. Inclusion terms: Group 1 peroxisomal disorders. Excludes1 (not coded here): Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.51-disorders-of-peroxisome-biogenesis"},{"code":"E71.510","title":"Zellweger syndrome","description":"Zellweger syndrome is a billable ICD-10-CM diagnosis code (E71.510). Excludes1 (not coded here): Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.510-zellweger-syndrome"},{"code":"E71.511","title":"Neonatal adrenoleukodystrophy","description":"Neonatal adrenoleukodystrophy is a billable ICD-10-CM diagnosis code (E71.511). Excludes1 (not coded here): X-linked adrenoleukodystrophy (E71.42-); Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.511-neonatal-adrenoleukodystrophy"},{"code":"E71.518","title":"Other disorders of peroxisome biogenesis","description":"Other disorders of peroxisome biogenesis is a billable ICD-10-CM diagnosis code (E71.518). Excludes1 (not coded here): Refsum's disease (G60.1); Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.518-other-disorders-of-peroxisome-biogenesis"},{"code":"E71.52","title":"X-linked adrenoleukodystrophy","description":"X-linked adrenoleukodystrophy is a non-billable ICD-10-CM category code (E71.52). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.52-x-linked-adrenoleukodystrophy"},{"code":"E71.520","title":"Childhood cerebral X-linked adrenoleukodystrophy","description":"Childhood cerebral X-linked adrenoleukodystrophy is a billable ICD-10-CM diagnosis code (E71.520). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.520-childhood-cerebral-x-linked-adrenoleukodystrophy"},{"code":"E71.521","title":"Adolescent X-linked adrenoleukodystrophy","description":"Adolescent X-linked adrenoleukodystrophy is a billable ICD-10-CM diagnosis code (E71.521). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.521-adolescent-x-linked-adrenoleukodystrophy"},{"code":"E71.522","title":"Adrenomyeloneuropathy","description":"Adrenomyeloneuropathy is a billable ICD-10-CM diagnosis code (E71.522). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.522-adrenomyeloneuropathy"},{"code":"E71.528","title":"Other X-linked adrenoleukodystrophy","description":"Other X-linked adrenoleukodystrophy is a billable ICD-10-CM diagnosis code (E71.528). Inclusion terms: Addison only phenotype adrenoleukodystrophy; Addison-Schilder adrenoleukodystrophy. Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.528-other-x-linked-adrenoleukodystrophy"},{"code":"E71.529","title":"X-linked adrenoleukodystrophy, unspecified type","description":"X-linked adrenoleukodystrophy, unspecified type is a billable ICD-10-CM diagnosis code (E71.529). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.529-x-linked-adrenoleukodystrophy-unspecified-type"},{"code":"E71.53","title":"Other group 2 peroxisomal disorders","description":"Other group 2 peroxisomal disorders is a billable ICD-10-CM diagnosis code (E71.53). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.53-other-group-2-peroxisomal-disorders"},{"code":"E71.54","title":"Other peroxisomal disorders","description":"Other peroxisomal disorders is a non-billable ICD-10-CM category code (E71.54). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e71.54-other-peroxisomal-disorders"},{"code":"E71.540","title":"Rhizomelic chondrodysplasia punctata","description":"Rhizomelic chondrodysplasia punctata is a billable ICD-10-CM diagnosis code (E71.540). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.540-rhizomelic-chondrodysplasia-punctata"},{"code":"E71.541","title":"Zellweger-like syndrome","description":"Zellweger-like syndrome is a billable ICD-10-CM diagnosis code (E71.541). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.541-zellweger-like-syndrome"},{"code":"E71.542","title":"Other group 3 peroxisomal disorders","description":"Other group 3 peroxisomal disorders is a billable ICD-10-CM diagnosis code (E71.542). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.542-other-group-3-peroxisomal-disorders"},{"code":"E71.548","title":"Other peroxisomal disorders","description":"Other peroxisomal disorders is a billable ICD-10-CM diagnosis code (E71.548). Excludes1 (not coded here): Schilder's disease (G37.0); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); hemolytic anemias attributable to enzyme disorders (D55.-); Marfan syndrome (Q87.4-); 5-alpha-reductase deficiency (E29.1). Excludes2 (not included here): Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e71.548-other-peroxisomal-disorders"}],"hierarchy":[],"relatedCodes":[],"relevantCPTCodes":[],"documentationTips":[],"caseStudies":[],"description":"","overview":""}