Showing codes E7881 (Lipoid dermatoarthritis) — E83824 (ABCC6 deficiency causing pseudoxanthoma elasticum)
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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ICD-10 Code: E805 (E80.5)
Code Type: Diagnosis
Description:
Crigler-Najjar syndrome
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ICD-10 Code: E806 (E80.6)
Code Type: Diagnosis
Description:
Other disorders of bilirubin metabolism
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ICD-10 Code: E807 (E80.7)
Code Type: Diagnosis
Description:
Disorder of bilirubin metabolism, unspecified
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ICD-10 Code: E83 (E83)
Code Type: Diagnosis
Description:
Disorders of mineral metabolism
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ICD-10 Code: E830 (E83.0)
Code Type: Diagnosis
Description:
Disorders of copper metabolism
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ICD-10 Code: E8300 (E83.00)
Code Type: Diagnosis
Description:
Disorder of copper metabolism, unspecified
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ICD-10 Code: E8301 (E83.01)
Code Type: Diagnosis
Description:
Wilson's disease
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ICD-10 Code: E8309 (E83.09)
Code Type: Diagnosis
Description:
Other disorders of copper metabolism
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ICD-10 Code: E831 (E83.1)
Code Type: Diagnosis
Description:
Disorders of iron metabolism
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ICD-10 Code: E8310 (E83.10)
Code Type: Diagnosis
Description:
Disorder of iron metabolism, unspecified
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ICD-10 Code: E8311 (E83.11)
Code Type: Diagnosis
Description:
Hemochromatosis
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ICD-10 Code: E83110 (E83.110)
Code Type: Diagnosis
Description:
Hereditary hemochromatosis
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ICD-10 Code: E83111 (E83.111)
Code Type: Diagnosis
Description:
Hemochromatosis due to repeated red blood cell transfusions
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ICD-10 Code: E83118 (E83.118)
Code Type: Diagnosis
Description:
Other hemochromatosis
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ICD-10 Code: E83119 (E83.119)
Code Type: Diagnosis
Description:
Hemochromatosis, unspecified
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ICD-10 Code: E8319 (E83.19)
Code Type: Diagnosis
Description:
Other disorders of iron metabolism
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ICD-10 Code: E832 (E83.2)
Code Type: Diagnosis
Description:
Disorders of zinc metabolism
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ICD-10 Code: E833 (E83.3)
Code Type: Diagnosis
Description:
Disorders of phosphorus metabolism and phosphatases
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ICD-10 Code: E8330 (E83.30)
Code Type: Diagnosis
Description:
Disorder of phosphorus metabolism, unspecified
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ICD-10 Code: E8331 (E83.31)
Code Type: Diagnosis
Description:
Familial hypophosphatemia
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ICD-10 Code: E8332 (E83.32)
Code Type: Diagnosis
Description:
Hereditary vitamin D-dependent rickets (type 1) (type 2)
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ICD-10 Code: E8339 (E83.39)
Code Type: Diagnosis
Description:
Other disorders of phosphorus metabolism
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ICD-10 Code: E834 (E83.4)
Code Type: Diagnosis
Description:
Disorders of magnesium metabolism
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ICD-10 Code: E8340 (E83.40)
Code Type: Diagnosis
Description:
Disorders of magnesium metabolism, unspecified
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ICD-10 Code: E8341 (E83.41)
Code Type: Diagnosis
Description:
Hypermagnesemia
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ICD-10 Code: E8342 (E83.42)
Code Type: Diagnosis
Description:
Hypomagnesemia
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ICD-10 Code: E8349 (E83.49)
Code Type: Diagnosis
Description:
Other disorders of magnesium metabolism
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ICD-10 Code: E835 (E83.5)
Code Type: Diagnosis
Description:
Disorders of calcium metabolism
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ICD-10 Code: E8350 (E83.50)
Code Type: Diagnosis
Description:
Unspecified disorder of calcium metabolism
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ICD-10 Code: E8351 (E83.51)
Code Type: Diagnosis
Description:
Hypocalcemia
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ICD-10 Code: E8352 (E83.52)
Code Type: Diagnosis
Description:
Hypercalcemia
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ICD-10 Code: E8359 (E83.59)
Code Type: Diagnosis
Description:
Other disorders of calcium metabolism
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ICD-10 Code: E838 (E83.8)
Code Type: Diagnosis
Description:
Other disorders of mineral metabolism
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ICD-10 Code: E8381 (E83.81)
Code Type: Diagnosis
Description:
Hungry bone syndrome
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ICD-10 Code: E8382 (E83.82)
Code Type: Diagnosis
Description:
Disorders of pyrophosphate metabolism
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ICD-10 Code: E83820 (E83.820)
Code Type: Diagnosis
Description:
Gen arterial calcifcn of infancy with unsp genetic causality (Generalized arterial calcification of infancy with unspecified genetic causality)
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ICD-10 Code: E83821 (E83.821)
Code Type: Diagnosis
Description:
ENPP1 deficiency causing gen arterial calcifcn of infancy (ENPP1 deficiency causing generalized arterial calcification of infancy)
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ICD-10 Code: E83822 (E83.822)
Code Type: Diagnosis
Description:
ENPP1 def cause autosom recess hypophosphate rickets type 2 (ENPP1 deficiency causing autosomal recessive hypophosphatemic rickets type 2)
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ICD-10 Code: E83823 (E83.823)
Code Type: Diagnosis
Description:
ABCC6 deficiency causing gen arterial calcifcn of infancy (ABCC6 deficiency causing generalized arterial calcification of infancy)
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ICD-10 Code: E83824 (E83.824)
Code Type: Diagnosis
Description:
ABCC6 deficiency causing pseudoxanthoma elasticum
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