ICD-10-CM codes

97,584 codes · page 101 of 1,952

ICD-10	Description
E803	Defects of catalase and peroxidase
E804	Gilbert syndrome
E805	Crigler-Najjar syndrome
E806	Other disorders of bilirubin metabolism
E807	Disorder of bilirubin metabolism, unspecified
E83	Disorders of mineral metabolism
E830	Disorders of copper metabolism
E8300	Disorder of copper metabolism, unspecified
E8301	Wilson's disease
E8309	Other disorders of copper metabolism
E831	Disorders of iron metabolism
E8310	Disorder of iron metabolism, unspecified
E8311	Hemochromatosis
E83110	Hereditary hemochromatosis
E83111	Hemochromatosis due to repeated red blood cell transfusions
E83118	Other hemochromatosis
E83119	Hemochromatosis, unspecified
E8319	Other disorders of iron metabolism
E832	Disorders of zinc metabolism
E833	Disorders of phosphorus metabolism and phosphatases
E8330	Disorder of phosphorus metabolism, unspecified
E8331	Familial hypophosphatemia
E8332	Hereditary vitamin D-dependent rickets (type 1) (type 2)
E8339	Other disorders of phosphorus metabolism
E834	Disorders of magnesium metabolism
E8340	Disorders of magnesium metabolism, unspecified
E8341	Hypermagnesemia
E8342	Hypomagnesemia
E8349	Other disorders of magnesium metabolism
E835	Disorders of calcium metabolism
E8350	Unspecified disorder of calcium metabolism
E8351	Hypocalcemia
E8352	Hypercalcemia
E8359	Other disorders of calcium metabolism
E838	Other disorders of mineral metabolism
E8381	Hungry bone syndrome
E8389	Other disorders of mineral metabolism
E839	Disorder of mineral metabolism, unspecified
E84	Cystic fibrosis
E840	Cystic fibrosis with pulmonary manifestations
E841	Cystic fibrosis with intestinal manifestations
E8411	Meconium ileus in cystic fibrosis
E8419	Cystic fibrosis with other intestinal manifestations
E848	Cystic fibrosis with other manifestations
E849	Cystic fibrosis, unspecified
E85	Amyloidosis
E850	Non-neuropathic heredofamilial amyloidosis
E851	Neuropathic heredofamilial amyloidosis
E852	Heredofamilial amyloidosis, unspecified
E853	Secondary systemic amyloidosis

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