Showing codes E7131 (Disorders of fatty-acid oxidation) — E7253 (Primary hyperoxaluria)
ICD-10 Code: E7131 (E71.31)
Code Type: Diagnosis
Description:
Disorders of fatty-acid oxidation
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ICD-10 Code: E71310 (E71.310)
Code Type: Diagnosis
Description:
Long chain/very long chain acyl CoA dehydrogenase deficiency
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ICD-10 Code: E71311 (E71.311)
Code Type: Diagnosis
Description:
Medium chain acyl CoA dehydrogenase deficiency
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ICD-10 Code: E71312 (E71.312)
Code Type: Diagnosis
Description:
Short chain acyl CoA dehydrogenase deficiency
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ICD-10 Code: E71313 (E71.313)
Code Type: Diagnosis
Description:
Glutaric aciduria type II
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ICD-10 Code: E71314 (E71.314)
Code Type: Diagnosis
Description:
Muscle carnitine palmitoyltransferase deficiency
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ICD-10 Code: E71318 (E71.318)
Code Type: Diagnosis
Description:
Other disorders of fatty-acid oxidation
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ICD-10 Code: E7132 (E71.32)
Code Type: Diagnosis
Description:
Disorders of ketone metabolism
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ICD-10 Code: E7139 (E71.39)
Code Type: Diagnosis
Description:
Other disorders of fatty-acid metabolism
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ICD-10 Code: E714 (E71.4)
Code Type: Diagnosis
Description:
Disorders of carnitine metabolism
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ICD-10 Code: E7140 (E71.40)
Code Type: Diagnosis
Description:
Disorder of carnitine metabolism, unspecified
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ICD-10 Code: E7141 (E71.41)
Code Type: Diagnosis
Description:
Primary carnitine deficiency
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ICD-10 Code: E7142 (E71.42)
Code Type: Diagnosis
Description:
Carnitine deficiency due to inborn errors of metabolism
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ICD-10 Code: E7143 (E71.43)
Code Type: Diagnosis
Description:
Iatrogenic carnitine deficiency
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ICD-10 Code: E7144 (E71.44)
Code Type: Diagnosis
Description:
Other secondary carnitine deficiency
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ICD-10 Code: E71440 (E71.440)
Code Type: Diagnosis
Description:
Ruvalcaba-Myhre-Smith syndrome
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ICD-10 Code: E71448 (E71.448)
Code Type: Diagnosis
Description:
Other secondary carnitine deficiency
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ICD-10 Code: E715 (E71.5)
Code Type: Diagnosis
Description:
Peroxisomal disorders
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ICD-10 Code: E7150 (E71.50)
Code Type: Diagnosis
Description:
Peroxisomal disorder, unspecified
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ICD-10 Code: E7151 (E71.51)
Code Type: Diagnosis
Description:
Disorders of peroxisome biogenesis
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ICD-10 Code: E71510 (E71.510)
Code Type: Diagnosis
Description:
Zellweger syndrome
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ICD-10 Code: E71511 (E71.511)
Code Type: Diagnosis
Description:
Neonatal adrenoleukodystrophy
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ICD-10 Code: E71518 (E71.518)
Code Type: Diagnosis
Description:
Other disorders of peroxisome biogenesis
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ICD-10 Code: E7152 (E71.52)
Code Type: Diagnosis
Description:
X-linked adrenoleukodystrophy
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ICD-10 Code: E71520 (E71.520)
Code Type: Diagnosis
Description:
Childhood cerebral X-linked adrenoleukodystrophy
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ICD-10 Code: E71521 (E71.521)
Code Type: Diagnosis
Description:
Adolescent X-linked adrenoleukodystrophy
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ICD-10 Code: E71522 (E71.522)
Code Type: Diagnosis
Description:
Adrenomyeloneuropathy
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ICD-10 Code: E71528 (E71.528)
Code Type: Diagnosis
Description:
Other X-linked adrenoleukodystrophy
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ICD-10 Code: E71529 (E71.529)
Code Type: Diagnosis
Description:
X-linked adrenoleukodystrophy, unspecified type
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ICD-10 Code: E7153 (E71.53)
Code Type: Diagnosis
Description:
Other group 2 peroxisomal disorders
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ICD-10 Code: E7154 (E71.54)
Code Type: Diagnosis
Description:
Other peroxisomal disorders
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ICD-10 Code: E71540 (E71.540)
Code Type: Diagnosis
Description:
Rhizomelic chondrodysplasia punctata
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ICD-10 Code: E71541 (E71.541)
Code Type: Diagnosis
Description:
Zellweger-like syndrome
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ICD-10 Code: E71542 (E71.542)
Code Type: Diagnosis
Description:
Other group 3 peroxisomal disorders
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ICD-10 Code: E71548 (E71.548)
Code Type: Diagnosis
Description:
Other peroxisomal disorders
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ICD-10 Code: E72 (E72)
Code Type: Diagnosis
Description:
Other disorders of amino-acid metabolism
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ICD-10 Code: E720 (E72.0)
Code Type: Diagnosis
Description:
Disorders of amino-acid transport
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ICD-10 Code: E7200 (E72.00)
Code Type: Diagnosis
Description:
Disorders of amino-acid transport, unspecified
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ICD-10 Code: E7201 (E72.01)
Code Type: Diagnosis
Description:
Cystinuria
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ICD-10 Code: E7202 (E72.02)
Code Type: Diagnosis
Description:
Hartnup's disease
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ICD-10 Code: E7203 (E72.03)
Code Type: Diagnosis
Description:
Lowe's syndrome
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ICD-10 Code: E7204 (E72.04)
Code Type: Diagnosis
Description:
Cystinosis
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ICD-10 Code: E7209 (E72.09)
Code Type: Diagnosis
Description:
Other disorders of amino-acid transport
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ICD-10 Code: E721 (E72.1)
Code Type: Diagnosis
Description:
Disorders of sulfur-bearing amino-acid metabolism
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ICD-10 Code: E7210 (E72.10)
Code Type: Diagnosis
Description:
Disorders of sulfur-bearing amino-acid metabolism, unsp (Disorders of sulfur-bearing amino-acid metabolism, unspecified)
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ICD-10 Code: E7211 (E72.11)
Code Type: Diagnosis
Description:
Homocystinuria
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ICD-10 Code: E7212 (E72.12)
Code Type: Diagnosis
Description:
Methylenetetrahydrofolate reductase deficiency
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ICD-10 Code: E7219 (E72.19)
Code Type: Diagnosis
Description:
Other disorders of sulfur-bearing amino-acid metabolism
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ICD-10 Code: E722 (E72.2)
Code Type: Diagnosis
Description:
Disorders of urea cycle metabolism
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ICD-10 Code: E7220 (E72.20)
Code Type: Diagnosis
Description:
Disorder of urea cycle metabolism, unspecified
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ICD-10 Code: E7221 (E72.21)
Code Type: Diagnosis
Description:
Argininemia
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ICD-10 Code: E7222 (E72.22)
Code Type: Diagnosis
Description:
Arginosuccinic aciduria
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ICD-10 Code: E7223 (E72.23)
Code Type: Diagnosis
Description:
Citrullinemia
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ICD-10 Code: E7229 (E72.29)
Code Type: Diagnosis
Description:
Other disorders of urea cycle metabolism
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ICD-10 Code: E723 (E72.3)
Code Type: Diagnosis
Description:
Disorders of lysine and hydroxylysine metabolism
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ICD-10 Code: E724 (E72.4)
Code Type: Diagnosis
Description:
Disorders of ornithine metabolism
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ICD-10 Code: E725 (E72.5)
Code Type: Diagnosis
Description:
Disorders of glycine metabolism
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ICD-10 Code: E7250 (E72.50)
Code Type: Diagnosis
Description:
Disorder of glycine metabolism, unspecified
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ICD-10 Code: E7251 (E72.51)
Code Type: Diagnosis
Description:
Non-ketotic hyperglycinemia
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ICD-10 Code: E7252 (E72.52)
Code Type: Diagnosis
Description:
Trimethylaminuria
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ICD-10 Code: E7253 (E72.53)
Code Type: Diagnosis
Description:
Primary hyperoxaluria
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