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 newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
- •disorders of tryptophan metabolismE70.5
Related Codes(5)
Also Known As / Clinical Terms(125)
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
UMLS
Clinical Terms
- Calculus chemical composition
- Lesion of bone
- Finding of calculus chemical composition
- X-linked vitamin D-resistant rickets
- Type II renal tubular acidosis
- Cystinemia
- Cystinaemia
- Dysplasia with defective mineralization
- Fanconi syndrome
- Microscopic nephrocalcinosis
- Disorder of tryptophan metabolism
- X-linked creatine deficiency
- Acquired Fanconi syndrome secondary to monoclonal gammopathy
- Bicarbonate reabsorption defect
- Beta-mercaptolactate cysteine disulfiduria
- Calculus chemical composition - finding
- Familial hypophosphatemic bone disease
- HPDR I - Hypophosphataemic vitamin D-resistant rickets
- Creatine transporter deficiency
- Iminoglycinuria
- Blue diaper syndrome
- Adult Fanconi syndrome
- Hereditary hypophosphataemia
- Neonatal renal disorder
- Familial hypophosphataemic osteomalacia
- Hereditary hypophosphatemia
- Atypical Fanconi syndrome, neonatal hyperinsulinism syndrome
- SLC6A8 related creatine transporter deficiency
- Familial vitamin D-resistant rickets
- Familial hypophosphataemic bone disease
- Familial x-linked hypophosphataemic vitamin D refractory rickets
- Proximal renal tubular acidosis
- Familial hypophosphataemia
- Dysplasia with defective mineralisation
- HPDR I - Hypophosphatemic vitamin D-resistant rickets
- Neonatal cystine-lysinuria
- Familial hypophosphatemic rickets
- Familial hypophosphatemic osteomalacia
- Tryptophan malabsorption syndrome
- Familial x-linked hypophosphatemic vitamin D refractory rickets
- Hypophosphatemic rickets with nephrotic-glycosuric dwarfism
- Familial hypophosphatemia
- Vitamin D-resistant rickets
- X-linked hypophosphataemic osteomalacia
- Glycinuria
- Renal tubular acidosis, type 2
- Familial renal iminoglycinuria
- Acquired Fanconi syndrome
- X-linked hypophosphatemic osteomalacia
- Familial hypophosphataemic rickets
- Renal tubular acidosis, rate type
- RTA (renal tubular acidosis) type II
- Vitamin D-resistant osteomalacia
- X-linked hypophosphataemic rickets
- Acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome
- Hypophosphataemic rickets with nephrotic-glycosuric dwarfism
- X-linked creatine deficiency syndrome
- X-linked hypophosphatemic rickets
- Fanconi (-de Toni) (-Debré) syndrome, unspecified
- Calculus = cystine
- Ampola syndrome
- Secondary Fanconi syndrome
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: 236467001, 724099000, 236468006, 784373007, 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.
How does E72.09 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of amino-acid transport affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E72.09?
There is no direct ICD-11 mapping available for E72.09 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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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.