2019 ICD-10-CM Diagnosis Code E72.09

Other disorders of amino-acid transport

    2016 2017 2018 2019 Billable/Specific Code
  • E72.09 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2019 edition of ICD-10-CM E72.09 became effective on October 1, 2018.
  • This is the American ICD-10-CM version of E72.09 - other international versions of ICD-10 E72.09 may differ.
Applicable To
  • Fanconi (-de Toni) (-Debré) syndrome, unspecified
The following code(s) above E72.09 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to E72.09:
  • E00-E89
    2019 ICD-10-CM Range E00-E89

    Endocrine, nutritional and metabolic diseases

    • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
    Type 1 Excludes
    • transitory endocrine and metabolic disorders specific to newborn (P70-P74)
    Endocrine, nutritional and metabolic diseases
  • E70-E88
    2019 ICD-10-CM Range E70-E88

    Metabolic disorders

    Type 1 Excludes
    • androgen insensitivity syndrome (E34.5-)
    • congenital adrenal hyperplasia (E25.0)
    • Ehlers-Danlos syndrome (Q79.6)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan's syndrome (Q87.4)
    • 5-alpha-reductase deficiency (E29.1)
    Metabolic disorders
  • E72
    ICD-10-CM Diagnosis Code E72

    Other disorders of amino-acid metabolism

      2016 2017 2018 2019 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • disorders of:
    • aromatic amino-acid metabolism (E70.-)
    • branched-chain amino-acid metabolism (E71.0-E71.2)
    • fatty-acid metabolism (E71.3)
    • purine and pyrimidine metabolism (E79.-)
    • gout (M1A.-, M10.-)
    Other disorders of amino-acid metabolism
  • E72.0
    ICD-10-CM Diagnosis Code E72.0

    Disorders of amino-acid transport

      2016 2017 2018 2019 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • disorders of tryptophan metabolism (E70.5)
    Disorders of amino-acid transport
Approximate Synonyms
  • Amino acid transport disorder
  • Disorder of amino acid transport
  • Fanconi syndrome
  • Glycinuria, 3 methylcrotonyl
  • Methylcrotonyl-coa carboxylase deficiency
ICD-10-CM E72.09 is grouped within Diagnostic Related Group(s) (MS-DRG v36.0):
  • 642 Inborn and other disorders of metabolism

Convert E72.09 to ICD-9-CM

Code History
  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
Code annotations containing back-references to E72.09:
  • Type 1 Excludes: E72.04
    ICD-10-CM Diagnosis Code E72.04


      2016 2017 2018 2019 Billable/Specific Code
    Applicable To
    • Fanconi (-de Toni) (-Debré) syndrome with cystinosis
    Type 1 Excludes
    • Fanconi (-de Toni) (-Debré) syndrome without cystinosis (E72.09)

Diagnosis Index entries containing back-references to E72.09:
  • Beta-mercaptolactate-cysteine disulfiduria E72.09
  • Blue
    • diaper syndrome E72.09
  • De Toni-Fanconi (-Debré) E72.09
  • Disorder (of) - see also Disease
    • amino-acid
      • glycinuria E72.09
      • renal transport NEC E72.09
      • transport NEC E72.09
  • Dwarfism E34.3
    ICD-10-CM Diagnosis Code E34.3

    Short stature due to endocrine disorder

      2016 2017 2018 2019 Billable/Specific Code
    Applicable To
    • Constitutional short stature
    • Laron-type short stature
    Type 1 Excludes
    • achondroplastic short stature (Q77.4)
    • hypochondroplastic short stature (Q77.4)
    • nutritional short stature (E45)
    • pituitary short stature (E23.0)
    • progeria (E34.8)
    • renal short stature (N25.0)
    • Russell-Silver syndrome (Q87.1)
    • short-limbed stature with immunodeficiency (D82.2)
    • short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
    • short stature NOS (R62.52)
    • nephrotic-glycosuric E72.09 (with hypophosphatemic rickets)
  • Fanconi (-de Toni)(-Debré) E72.09
  • Glycinuria E72.09 (renal) (with ketosis)
  • Lignac (-de Toni) (-Fanconi) (-Debré) E72.09
  • Rickets (active) (acute) (adolescent) (chest wall) (congenital) (current) (infantile) (intestinal) E55.0
    ICD-10-CM Diagnosis Code E55.0

    Rickets, active

      2016 2017 2018 2019 Billable/Specific Code
    Applicable To
    • Infantile osteomalacia
    • Juvenile osteomalacia
    Type 1 Excludes
    • celiac rickets (K90.0)
    • Crohn's rickets (K50.-)
    • hereditary vitamin D-dependent rickets (E83.32)
    • inactive rickets (E64.3)
    • renal rickets (N25.0)
    • sequelae of rickets (E64.3)
    • vitamin D-resistant rickets (E83.31)
    • hypophosphatemic with nephrotic-glycosuric dwarfism E72.09
  • Sclerosis, sclerotic
    • renal N26.9
      ICD-10-CM Diagnosis Code N26.9

      Renal sclerosis, unspecified

        2016 2017 2018 2019 Billable/Specific Code
      • with
        • cystine storage disease E72.09
  • Stone(s) - see also Calculus
    • cystine E72.09
  • Syndrome - see also Disease
  • Toni-Fanconi syndrome (cystinosis) E72.09

ICD-10-CM Codes Adjacent To E72.09
E71.541 Zellweger-like syndrome
E71.542 Other group 3 peroxisomal disorders
E71.548 Other peroxisomal disorders
E72 Other disorders of amino-acid metabolism
E72.0 Disorders of amino-acid transport
E72.00 …… unspecified
E72.01 Cystinuria
E72.02 Hartnup's disease
E72.03 Lowe's syndrome
E72.04 Cystinosis
E72.09 Other disorders of amino-acid transport
E72.1 Disorders of sulfur-bearing amino-acid metabolism
E72.10 …… unspecified
E72.11 Homocystinuria
E72.12 Methylenetetrahydrofolate reductase deficiency
E72.19 Other disorders of sulfur-bearing amino-acid metabolism
E72.2 Disorders of urea cycle metabolism
E72.20 Disorder of urea cycle metabolism, unspecified
E72.21 Argininemia
E72.22 Arginosuccinic aciduria
E72.23 Citrullinemia

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.