Showing codes E7033 (Albinism with hematologic abnormality) — E7154 (Other peroxisomal disorders)

ICD-10 Code: E7033 (E70.33)
Code Type: Diagnosis
Description:
Albinism with hematologic abnormality

HTML  |  TXT  |  Mapping ICD-10 Code: E70330 (E70.330)
Code Type: Diagnosis
Description:
Chediak-Higashi syndrome

HTML  |  TXT  |  Mapping ICD-10 Code: E70331 (E70.331)
Code Type: Diagnosis
Description:
Hermansky-Pudlak syndrome

HTML  |  TXT  |  Mapping ICD-10 Code: E70338 (E70.338)
Code Type: Diagnosis
Description:
Other albinism with hematologic abnormality

HTML  |  TXT  |  Mapping ICD-10 Code: E70339 (E70.339)
Code Type: Diagnosis
Description:
Albinism with hematologic abnormality, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E7039 (E70.39)
Code Type: Diagnosis
Description:
Other specified albinism

HTML  |  TXT  |  Mapping ICD-10 Code: E704 (E70.4)
Code Type: Diagnosis
Description:
Disorders of histidine metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7040 (E70.40)
Code Type: Diagnosis
Description:
Disorders of histidine metabolism, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E7041 (E70.41)
Code Type: Diagnosis
Description:
Histidinemia

HTML  |  TXT  |  Mapping ICD-10 Code: E7049 (E70.49)
Code Type: Diagnosis
Description:
Other disorders of histidine metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E705 (E70.5)
Code Type: Diagnosis
Description:
Disorders of tryptophan metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E708 (E70.8)
Code Type: Diagnosis
Description:
Other disorders of aromatic amino-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7081 (E70.81)
Code Type: Diagnosis
Description:
Aromatic L-amino acid decarboxylase deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E7089 (E70.89)
Code Type: Diagnosis
Description:
Other disorders of aromatic amino-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E709 (E70.9)
Code Type: Diagnosis
Description:
Disorder of aromatic amino-acid metabolism, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E71 (E71)
Code Type: Diagnosis
Description:
Disord of branched-chain amino-acid metab & fatty-acid metab (Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism)

HTML  |  TXT  |  Mapping ICD-10 Code: E710 (E71.0)
Code Type: Diagnosis
Description:
Maple-syrup-urine disease

HTML  |  TXT  |  Mapping ICD-10 Code: E711 (E71.1)
Code Type: Diagnosis
Description:
Other disorders of branched-chain amino-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7111 (E71.11)
Code Type: Diagnosis
Description:
Branched-chain organic acidurias

HTML  |  TXT  |  Mapping ICD-10 Code: E71110 (E71.110)
Code Type: Diagnosis
Description:
Isovaleric acidemia

HTML  |  TXT  |  Mapping ICD-10 Code: E71111 (E71.111)
Code Type: Diagnosis
Description:
3-methylglutaconic aciduria

HTML  |  TXT  |  Mapping ICD-10 Code: E71118 (E71.118)
Code Type: Diagnosis
Description:
Other branched-chain organic acidurias

HTML  |  TXT  |  Mapping ICD-10 Code: E7112 (E71.12)
Code Type: Diagnosis
Description:
Disorders of propionate metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E71120 (E71.120)
Code Type: Diagnosis
Description:
Methylmalonic acidemia

HTML  |  TXT  |  Mapping ICD-10 Code: E71121 (E71.121)
Code Type: Diagnosis
Description:
Propionic acidemia

HTML  |  TXT  |  Mapping ICD-10 Code: E71128 (E71.128)
Code Type: Diagnosis
Description:
Other disorders of propionate metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7119 (E71.19)
Code Type: Diagnosis
Description:
Other disorders of branched-chain amino-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E712 (E71.2)
Code Type: Diagnosis
Description:
Disorder of branched-chain amino-acid metabolism, unsp (Disorder of branched-chain amino-acid metabolism, unspecified)

HTML  |  TXT  |  Mapping ICD-10 Code: E713 (E71.3)
Code Type: Diagnosis
Description:
Disorders of fatty-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7130 (E71.30)
Code Type: Diagnosis
Description:
Disorder of fatty-acid metabolism, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E7131 (E71.31)
Code Type: Diagnosis
Description:
Disorders of fatty-acid oxidation

HTML  |  TXT  |  Mapping ICD-10 Code: E71310 (E71.310)
Code Type: Diagnosis
Description:
Long chain/very long chain acyl CoA dehydrogenase deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E71311 (E71.311)
Code Type: Diagnosis
Description:
Medium chain acyl CoA dehydrogenase deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E71312 (E71.312)
Code Type: Diagnosis
Description:
Short chain acyl CoA dehydrogenase deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E71313 (E71.313)
Code Type: Diagnosis
Description:
Glutaric aciduria type II

HTML  |  TXT  |  Mapping ICD-10 Code: E71314 (E71.314)
Code Type: Diagnosis
Description:
Muscle carnitine palmitoyltransferase deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E71318 (E71.318)
Code Type: Diagnosis
Description:
Other disorders of fatty-acid oxidation

HTML  |  TXT  |  Mapping ICD-10 Code: E7132 (E71.32)
Code Type: Diagnosis
Description:
Disorders of ketone metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7139 (E71.39)
Code Type: Diagnosis
Description:
Other disorders of fatty-acid metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E714 (E71.4)
Code Type: Diagnosis
Description:
Disorders of carnitine metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7140 (E71.40)
Code Type: Diagnosis
Description:
Disorder of carnitine metabolism, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E7141 (E71.41)
Code Type: Diagnosis
Description:
Primary carnitine deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E7142 (E71.42)
Code Type: Diagnosis
Description:
Carnitine deficiency due to inborn errors of metabolism

HTML  |  TXT  |  Mapping ICD-10 Code: E7143 (E71.43)
Code Type: Diagnosis
Description:
Iatrogenic carnitine deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E7144 (E71.44)
Code Type: Diagnosis
Description:
Other secondary carnitine deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E71440 (E71.440)
Code Type: Diagnosis
Description:
Ruvalcaba-Myhre-Smith syndrome

HTML  |  TXT  |  Mapping ICD-10 Code: E71448 (E71.448)
Code Type: Diagnosis
Description:
Other secondary carnitine deficiency

HTML  |  TXT  |  Mapping ICD-10 Code: E715 (E71.5)
Code Type: Diagnosis
Description:
Peroxisomal disorders

HTML  |  TXT  |  Mapping ICD-10 Code: E7150 (E71.50)
Code Type: Diagnosis
Description:
Peroxisomal disorder, unspecified

HTML  |  TXT  |  Mapping ICD-10 Code: E7151 (E71.51)
Code Type: Diagnosis
Description:
Disorders of peroxisome biogenesis

HTML  |  TXT  |  Mapping ICD-10 Code: E71510 (E71.510)
Code Type: Diagnosis
Description:
Zellweger syndrome

HTML  |  TXT  |  Mapping ICD-10 Code: E71511 (E71.511)
Code Type: Diagnosis
Description:
Neonatal adrenoleukodystrophy

HTML  |  TXT  |  Mapping ICD-10 Code: E71518 (E71.518)
Code Type: Diagnosis
Description:
Other disorders of peroxisome biogenesis

HTML  |  TXT  |  Mapping ICD-10 Code: E7152 (E71.52)
Code Type: Diagnosis
Description:
X-linked adrenoleukodystrophy

HTML  |  TXT  |  Mapping ICD-10 Code: E71520 (E71.520)
Code Type: Diagnosis
Description:
Childhood cerebral X-linked adrenoleukodystrophy

HTML  |  TXT  |  Mapping ICD-10 Code: E71521 (E71.521)
Code Type: Diagnosis
Description:
Adolescent X-linked adrenoleukodystrophy

HTML  |  TXT  |  Mapping ICD-10 Code: E71522 (E71.522)
Code Type: Diagnosis
Description:
Adrenomyeloneuropathy

HTML  |  TXT  |  Mapping ICD-10 Code: E71528 (E71.528)
Code Type: Diagnosis
Description:
Other X-linked adrenoleukodystrophy

HTML  |  TXT  |  Mapping ICD-10 Code: E71529 (E71.529)
Code Type: Diagnosis
Description:
X-linked adrenoleukodystrophy, unspecified type

HTML  |  TXT  |  Mapping ICD-10 Code: E7153 (E71.53)
Code Type: Diagnosis
Description:
Other group 2 peroxisomal disorders

HTML  |  TXT  |  Mapping ICD-10 Code: E7154 (E71.54)
Code Type: Diagnosis
Description:
Other peroxisomal disorders

HTML  |  TXT  |  Mapping
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