Diagnosis Code: 270.0

Short Description: Amino-acid transport dis

Long Description: Disturbances of amino-acid transport

Code Classification:

• Endocrine, nutritional and metabolic diseases, and immunity disorders (240–279)
  • Other metabolic disorders and immunity disorders (270-279)
    • 270 Disorders of amino-acid transport and metabolism
      • 270.0 Amino-acid transport dis

Code Version: 2015 ICD-9-CM

References to Index of Diseases and Injuries

The code 270.0 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Abderhalden-Kaufmann-Lignac syndrome (cystinosis) 270.0

• Beta-mercaptolactate-cysteine disulfiduria 270.0

• Blue
  • diaper syndrome 270.0

• Cystinosis (malignant) 270.0

• Cystinuria 270.0

• Deficiency, deficient
  • sulfite oxidase 270.0

• Deposit
  • cornea, corneal NEC 371.10
    • in
      • cystinosis 270.0 [371.15]

• de Toni-Fanconi syndrome (cystinosis) 270.0

• Diathesis
  • cystine (familial) 270.0

• Disease, diseased - see also Syndrome
  • cystine storage (with renal sclerosis) 270.0
  • H 270.0
  • Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
  • Hartnup (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
  • Lignac's (cystinosis) 270.0

• Disorder - see also Disease
  • amino acid (metabolic) (see also Disturbance, metabolism, amino acid) 270.9
    • cystinosis 270.0
    • cystinuria 270.0
    • glycinuria 270.0
    • renal transport NEC 270.0
    • transport NEC 270.0
      • renal 270.0
  • metabolism NEC 277.9
    • cystine storage 270.0
    • cystinuria 270.0

• Disturbance - see also Disease
  • amino acid (metabolic) (see also Disorder, amino acid) 270.9
    • transport 270.0
  • metabolism (acquired) (congenital) (see also Disorder, metabolism) 277.9
    • amino acid (see also Disorder, amino acid) 270.9
      • transport 270.0

• Disulfiduria, beta-mercaptolactate-cysteine 270.0

• Dwarf, dwarfism 259.4
  • nephrotic-glycosuric, with hypophosphatemic rickets 270.0

• Fanconi (-de Toni) (-Debr�) syndrome (cystinosis) 270.0

• Glycinuria (renal) (with ketosis) 270.0

• Hart's disease or syndrome (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0

• Hartnup disease (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0

• H disease 270.0

• Hyperaminoaciduria 270.9
  • cystine 270.0
  • glycine 270.0
  • renal (types I, II, III) 270.0

• Lignac's disease (cystinosis) 270.0

• Lignac (-de Toni) (-Fanconi) (-Debr�) syndrome (cystinosis) 270.0

• Lignac (-Fanconi) syndrome (cystinosis) 270.0

• Pellagra-cerebellar-ataxia-renal aminoaciduria syndrome 270.0

• Rickets (active) (acute) (adolescent) (adult) (chest wall) (congenital) (current) (infantile) (intestinal) 268.0
  • hypophosphatemic with nephrotic-glycosuric dwarfism 270.0

• Sclerosis, sclerotic
  • renal 587
    • with
      • cystine storage disease 270.0

• Stone(s) - see also Calculus
  • cystine 270.0

• Syndrome - see also Disease
  • blue
    • diaper 270.0
  • de Toni-Fanconi (-Debre) (cystinosis) 270.0
  • Fanconi (-de Toni) (-Debr�) (cystinosis) 270.0
  • Hart's (pellagra-cerebellar ataxia-renal aminoaciduria) 270.0
  • Lignac (-de Toni) (-Fanconi) (-Debr�) (cystinosis) 270.0
  • pellagra-cerebellar ataxia-renal aminoaciduria 270.0
  • Toni-Fanconi (cystinosis) 270.0

• Thesaurismosis
  • cystine 270.0

• Toni-Fanconi syndrome (cystinosis) 270.0

Crosswalk Information

The code 270.0 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

« Previous Code