{"code":"E83","type":"category","title":"Disorders of mineral metabolism","codeAlso":[],"includes":[],"modern_v":"official26","codeFirst":[],"excludes1":["dietary mineral deficiency (E58-E61)","parathyroid disorders (E20-E21)","vitamin D deficiency (E55.-)","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,"fyEffectivity":{"fy2026":true,"fy2027":true,"billableFy2026":false,"billableFy2027":false},"sibling_codes":["E83.0","E83.01","E83.09","E83.1","E83.10","E83.11","E83.110","E83.111","E83.118","E83.119","E83.19","E83.2","E83.3","E83.30","E83.31","E83.32","E83.39","E83.4","E83.40","E83.41","E83.42","E83.49","E83.5","E83.50","E83.51","E83.52","E83.59","E83.8","E83.81","E83.82","E83.820","E83.821","E83.822","E83.823","E83.824","E83.825","E83.89","E83.9"],"inclusionTerms":[],"sibling_titles":{"code":"E83.9","title":"Disorder of mineral metabolism, unspecified","isBillable":true},"useAdditionalCode":[],"clinicalDefinition":"Disorders of mineral metabolism is a non-billable ICD-10-CM category code (E83). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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 mineral metabolism is a non-billable ICD-10-CM category code (E83). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"E83.0","title":"Disorders of copper metabolism","description":"Disorders of copper metabolism is a non-billable ICD-10-CM category code (E83.0). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.0-disorders-of-copper-metabolism"},{"code":"E83.00","title":"Disorder of copper metabolism, unspecified","description":"Disorder of copper metabolism, unspecified is a billable ICD-10-CM diagnosis code (E83.00). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.00-disorder-of-copper-metabolism-unspecified"},{"code":"E83.01","title":"Wilson's disease","description":"Wilson's disease is a billable ICD-10-CM diagnosis code (E83.01). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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 Kayser Fleischer ring (H18.04-).","isBillable":true,"slug":"e83.01-wilsons-disease"},{"code":"E83.09","title":"Other disorders of copper metabolism","description":"Other disorders of copper metabolism is a billable ICD-10-CM diagnosis code (E83.09). Inclusion terms: Menkes' (kinky hair) (steely hair) disease. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.09-other-disorders-of-copper-metabolism"},{"code":"E83.1","title":"Disorders of iron metabolism","description":"Disorders of iron metabolism is a non-billable ICD-10-CM category code (E83.1). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.1-disorders-of-iron-metabolism"},{"code":"E83.10","title":"Disorder of iron metabolism, unspecified","description":"Disorder of iron metabolism, unspecified is a billable ICD-10-CM diagnosis code (E83.10). Excludes1 (not coded here): iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.10-disorder-of-iron-metabolism-unspecified"},{"code":"E83.11","title":"Hemochromatosis","description":"Hemochromatosis is a non-billable ICD-10-CM category code (E83.11). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.11-hemochromatosis"},{"code":"E83.110","title":"Hereditary hemochromatosis","description":"Hereditary hemochromatosis is a billable ICD-10-CM diagnosis code (E83.110). Inclusion terms: Bronzed diabetes; Pigmentary cirrhosis (of liver); Primary (hereditary) hemochromatosis. Excludes1 (not coded here): GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.110-hereditary-hemochromatosis"},{"code":"E83.111","title":"Hemochromatosis due to repeated red blood cell transfusions","description":"Hemochromatosis due to repeated red blood cell transfusions is a billable ICD-10-CM diagnosis code (E83.111). Inclusion terms: Iron overload due to repeated red blood cell transfusions; Transfusion (red blood cell) associated hemochromatosis. Excludes1 (not coded here): GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.111-hemochromatosis-due-to-repeated-red-blood-cell-transfusions"},{"code":"E83.118","title":"Other hemochromatosis","description":"Other hemochromatosis is a billable ICD-10-CM diagnosis code (E83.118). Excludes1 (not coded here): GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.118-other-hemochromatosis"},{"code":"E83.119","title":"Hemochromatosis, unspecified","description":"Hemochromatosis, unspecified is a billable ICD-10-CM diagnosis code (E83.119). Excludes1 (not coded here): GALD (P78.84); Gestational alloimmune liver disease (P78.84); Neonatal hemochromatosis (P78.84); iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.119-hemochromatosis-unspecified"},{"code":"E83.19","title":"Other disorders of iron metabolism","description":"Other disorders of iron metabolism is a billable ICD-10-CM diagnosis code (E83.19). Excludes1 (not coded here): iron deficiency anemia (D50.-); sideroblastic anemia (D64.0-D64.3); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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-). Use additional code: code, if applicable, for idiopathic pulmonary hemosiderosis (J84.03).","isBillable":true,"slug":"e83.19-other-disorders-of-iron-metabolism"},{"code":"E83.2","title":"Disorders of zinc metabolism","description":"Disorders of zinc metabolism is a billable ICD-10-CM diagnosis code (E83.2). Inclusion terms: Acrodermatitis enteropathica. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.2-disorders-of-zinc-metabolism"},{"code":"E83.3","title":"Disorders of phosphorus metabolism and phosphatases","description":"Disorders of phosphorus metabolism and phosphatases is a non-billable ICD-10-CM category code (E83.3). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","isBillable":false,"slug":"e83.3-disorders-of-phosphorus-metabolism-and-phosphatases"},{"code":"E83.30","title":"Disorder of phosphorus metabolism, unspecified","description":"Disorder of phosphorus metabolism, unspecified is a billable ICD-10-CM diagnosis code (E83.30). Excludes1 (not coded here): adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e83.30-disorder-of-phosphorus-metabolism-unspecified"},{"code":"E83.31","title":"Familial hypophosphatemia","description":"Familial hypophosphatemia is a billable ICD-10-CM diagnosis code (E83.31). Inclusion terms: Vitamin D-resistant osteomalacia; Vitamin D-resistant rickets. Excludes1 (not coded here): vitamin D-deficiency rickets (E55.0); adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e83.31-familial-hypophosphatemia"},{"code":"E83.32","title":"Hereditary vitamin D-dependent rickets (type 1) (type 2)","description":"Hereditary vitamin D-dependent rickets (type 1) (type 2) is a billable ICD-10-CM diagnosis code (E83.32). Inclusion terms: 25-hydroxyvitamin D 1-alpha-hydroxylase deficiency; Pseudovitamin D deficiency; Vitamin D receptor defect. Excludes1 (not coded here): adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e83.32-hereditary-vitamin-d-dependent-rickets-type-1-type-2"},{"code":"E83.39","title":"Other disorders of phosphorus metabolism","description":"Other disorders of phosphorus metabolism is a billable ICD-10-CM diagnosis code (E83.39). Inclusion terms: Acid phosphatase deficiency; Hypophosphatasia. Excludes1 (not coded here): adult osteomalacia (M83.-); osteoporosis (M80.-); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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): disorders of pyrophosphate metabolism (E83.82-); Ehlers-Danlos syndromes (Q79.6-).","isBillable":true,"slug":"e83.39-other-disorders-of-phosphorus-metabolism"},{"code":"E83.4","title":"Disorders of magnesium metabolism","description":"Disorders of magnesium metabolism is a non-billable ICD-10-CM category code (E83.4). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.4-disorders-of-magnesium-metabolism"},{"code":"E83.40","title":"Disorders of magnesium metabolism, unspecified","description":"Disorders of magnesium metabolism, unspecified is a billable ICD-10-CM diagnosis code (E83.40). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.40-disorders-of-magnesium-metabolism-unspecified"},{"code":"E83.41","title":"Hypermagnesemia","description":"Hypermagnesemia is a billable ICD-10-CM diagnosis code (E83.41). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.41-hypermagnesemia"},{"code":"E83.42","title":"Hypomagnesemia","description":"Hypomagnesemia is a billable ICD-10-CM diagnosis code (E83.42). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.42-hypomagnesemia"},{"code":"E83.49","title":"Other disorders of magnesium metabolism","description":"Other disorders of magnesium metabolism is a billable ICD-10-CM diagnosis code (E83.49). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.49-other-disorders-of-magnesium-metabolism"},{"code":"E83.5","title":"Disorders of calcium metabolism","description":"Disorders of calcium metabolism is a non-billable ICD-10-CM category code (E83.5). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): autoimmune hypoparathyroidism (E20.812); autosomal dominant hypocalcemia (E20.810); chondrocalcinosis (M11.1-M11.2); hungry bone syndrome (E83.81); hyperparathyroidism (E21.0-E21.3); secondary hypoparathyroidism in diseases classified elsewhere (E20.811); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.5-disorders-of-calcium-metabolism"},{"code":"E83.50","title":"Unspecified disorder of calcium metabolism","description":"Unspecified disorder of calcium metabolism is a billable ICD-10-CM diagnosis code (E83.50). Excludes1 (not coded here): autoimmune hypoparathyroidism (E20.812); autosomal dominant hypocalcemia (E20.810); chondrocalcinosis (M11.1-M11.2); hungry bone syndrome (E83.81); hyperparathyroidism (E21.0-E21.3); secondary hypoparathyroidism in diseases classified elsewhere (E20.811); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.50-unspecified-disorder-of-calcium-metabolism"},{"code":"E83.51","title":"Hypocalcemia","description":"Hypocalcemia is a billable ICD-10-CM diagnosis code (E83.51). Excludes1 (not coded here): autoimmune hypoparathyroidism (E20.812); autosomal dominant hypocalcemia (E20.810); chondrocalcinosis (M11.1-M11.2); hungry bone syndrome (E83.81); hyperparathyroidism (E21.0-E21.3); secondary hypoparathyroidism in diseases classified elsewhere (E20.811); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.51-hypocalcemia"},{"code":"E83.52","title":"Hypercalcemia","description":"Hypercalcemia is a billable ICD-10-CM diagnosis code (E83.52). Inclusion terms: Familial hypocalciuric hypercalcemia. Excludes1 (not coded here): autoimmune hypoparathyroidism (E20.812); autosomal dominant hypocalcemia (E20.810); chondrocalcinosis (M11.1-M11.2); hungry bone syndrome (E83.81); hyperparathyroidism (E21.0-E21.3); secondary hypoparathyroidism in diseases classified elsewhere (E20.811); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.52-hypercalcemia"},{"code":"E83.59","title":"Other disorders of calcium metabolism","description":"Other disorders of calcium metabolism is a billable ICD-10-CM diagnosis code (E83.59). Excludes1 (not coded here): autoimmune hypoparathyroidism (E20.812); autosomal dominant hypocalcemia (E20.810); chondrocalcinosis (M11.1-M11.2); hungry bone syndrome (E83.81); hyperparathyroidism (E21.0-E21.3); secondary hypoparathyroidism in diseases classified elsewhere (E20.811); dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.59-other-disorders-of-calcium-metabolism"},{"code":"E83.8","title":"Other disorders of mineral metabolism","description":"Other disorders of mineral metabolism is a non-billable ICD-10-CM category code (E83.8). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.8-other-disorders-of-mineral-metabolism"},{"code":"E83.81","title":"Hungry bone syndrome","description":"Hungry bone syndrome is a billable ICD-10-CM diagnosis code (E83.81). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.81-hungry-bone-syndrome"},{"code":"E83.82","title":"Disorders of pyrophosphate metabolism","description":"Disorders of pyrophosphate metabolism is a non-billable ICD-10-CM category code (E83.82). A more specific billable subcode must be selected for claims submission. Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.82-disorders-of-pyrophosphate-metabolism"},{"code":"E83.820","title":"Generalized arterial calcification of infancy with unspecified genetic causality","description":"Generalized arterial calcification of infancy with unspecified genetic causality is a billable ICD-10-CM diagnosis code (E83.820). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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: , if applicable, associated conditions such as:; heart failure (I50.-); other secondary hypertension (I15.8).","isBillable":true,"slug":"e83.820-generalized-arterial-calcification-of-infancy-with-unspecified-genetic-causality"},{"code":"E83.821","title":"ENPP1 deficiency causing generalized arterial calcification of infancy","description":"ENPP1 deficiency causing generalized arterial calcification of infancy is a billable ICD-10-CM diagnosis code (E83.821). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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: , if applicable, associated conditions such as:; heart failure (I50.-); other secondary hypertension (I15.8).","isBillable":true,"slug":"e83.821-enpp1-deficiency-causing-generalized-arterial-calcification-of-infancy"},{"code":"E83.822","title":"ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2","description":"ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2 is a billable ICD-10-CM diagnosis code (E83.822). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.822-enpp1-deficiency-causing-autosomal-recessive-hypophosphatemic-rickets-type-2"},{"code":"E83.823","title":"ABCC6 deficiency causing generalized arterial calcification of infancy","description":"ABCC6 deficiency causing generalized arterial calcification of infancy is a billable ICD-10-CM diagnosis code (E83.823). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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: , if applicable, associated conditions such as:; heart failure (I50.-); other secondary hypertension (I15.8).","isBillable":true,"slug":"e83.823-abcc6-deficiency-causing-generalized-arterial-calcification-of-infancy"},{"code":"E83.824","title":"ABCC6 deficiency causing pseudoxanthoma elasticum","description":"ABCC6 deficiency causing pseudoxanthoma elasticum is a billable ICD-10-CM diagnosis code (E83.824). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.824-abcc6-deficiency-causing-pseudoxanthoma-elasticum"},{"code":"E83.825","title":"CD73 deficiency causing arterial calcification","description":"CD73 deficiency causing arterial calcification is a billable ICD-10-CM diagnosis code (E83.825). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.825-cd73-deficiency-causing-arterial-calcification"},{"code":"E83.89","title":"Other disorders of mineral metabolism","description":"Other disorders of mineral metabolism is a billable ICD-10-CM diagnosis code (E83.89). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.89-other-disorders-of-mineral-metabolism"},{"code":"E83.9","title":"Disorder of mineral metabolism, unspecified","description":"Disorder of mineral metabolism, unspecified is a billable ICD-10-CM diagnosis code (E83.9). Excludes1 (not coded here): dietary mineral deficiency (E58-E61); parathyroid disorders (E20-E21); vitamin D deficiency (E55.-); 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":"e83.9-disorder-of-mineral-metabolism-unspecified"}],"hierarchy":[],"relatedCodes":[],"relevantCPTCodes":[],"documentationTips":[],"caseStudies":[],"description":"","overview":""}