E72.09
BillableOther disorders of amino-acid transport
Other disorders of amino-acid transport
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Fanconi (-de Toni) (-Debré) syndrome, unspecified
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- androgen insensitivity syndrome (E34.5-)
- congenital adrenal hyperplasia (E25.0)
- hemolytic anemias attributable to enzyme disorders (D55.-)
- Marfan syndrome (Q87.4-)
- 5-alpha-reductase deficiency (E29.1)
- 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.-)
- disorders of tryptophan metabolism (E70.5)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Disorder of tryptophan metabolism5181007
- Bicarbonate reabsorption defect24790002
- Proximal renal tubular acidosis24790002
- RTA (renal tubular acidosis) type II24790002
- Renal tubular acidosis, rate type24790002
- Renal tubular acidosis, type 224790002
- Type II renal tubular acidosis24790002
- Neonatal cystine-lysinuria30101004
- Fanconi syndrome40488004
- Blue diaper syndrome59531002
- Tryptophan malabsorption syndrome59531002
- Familial renal iminoglycinuria75652008
- Familial hypophosphataemia82236004
- Familial hypophosphataemic bone disease82236004
- Familial hypophosphataemic osteomalacia82236004
- Familial hypophosphataemic rickets82236004
- Familial hypophosphatemia82236004
- Familial hypophosphatemic bone disease82236004
- Familial hypophosphatemic osteomalacia82236004
- Familial hypophosphatemic rickets82236004
- Familial vitamin D-resistant rickets82236004
- Familial x-linked hypophosphataemic vitamin D refractory rickets82236004
- Familial x-linked hypophosphatemic vitamin D refractory rickets82236004
- HPDR I - Hypophosphataemic vitamin D-resistant rickets82236004
- HPDR I - Hypophosphatemic vitamin D-resistant rickets82236004
- Hereditary hypophosphataemia82236004
- Hereditary hypophosphatemia82236004
- Vitamin D-resistant osteomalacia82236004
- Vitamin D-resistant rickets82236004
- X-linked hypophosphataemic osteomalacia82236004
- X-linked hypophosphataemic rickets82236004
- X-linked hypophosphatemic osteomalacia82236004
- X-linked hypophosphatemic rickets82236004
- X-linked vitamin D-resistant rickets82236004
- Iminoglycinuria84121007
- Cystinaemia190682005
- Cystinemia190682005
- Microscopic nephrocalcinosis236444003
- Acquired Fanconi syndrome236467001
- Secondary Fanconi syndrome236467001
- Adult Fanconi syndrome236468006
- Glycinuria236477004
- Hypophosphataemic rickets with nephrotic-glycosuric dwarfism237888005
- Hypophosphatemic rickets with nephrotic-glycosuric dwarfism237888005
- Dysplasia with defective mineralisation254117007
- Dysplasia with defective mineralization254117007
- Neonatal renal disorder363224005
- Calculus chemical composition365789002
- Calculus chemical composition - finding365789002
- Finding of calculus chemical composition365789002
- Calculus = cystine384949003
- Creatine transporter deficiency698290008
- SLC6A8 related creatine transporter deficiency698290008
- X-linked creatine deficiency698290008
- X-linked creatine deficiency syndrome698290008
- Acquired Fanconi syndrome secondary to monoclonal gammopathy724099000
- Acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome724099000
- Ampola syndrome784373007
- Beta-mercaptolactate cysteine disulfiduria784373007
- Lesion of bone879976004
- Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome1269271003
Frequently Asked Questions
What is the ICD-10 code for other disorders of amino-acid transport?
The ICD-10-CM code for other disorders of amino-acid transport is E72.09. The full clinical description is "Other disorders of amino-acid transport". E72.09 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.09 mean?
ICD-10-CM code E72.09 represents "Other disorders of amino-acid transport". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E72.09 a billable code?
Yes, E72.09 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.09 in?
E72.09 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.09?
E72.09 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 10 more.
What SNOMED CT codes does E72.09 map to?
E72.09 maps to 23 SNOMED CT concepts: 784373007, 236467001, 724099000, 236468006, 1269271003, and 18 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.09?
E72.09 is linked to 2 UMLS Concept Unique Identifiers: C2874258, C2874259. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.