AutoICD API

E72.3

Billable

Disorders of lysine and hydroxylysine metabolism

Disorders of lysine and hydroxylysine metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E72

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Glutaric aciduria NOS
  • Glutaric aciduria (type I)
  • Hydroxylysinemia
  • Hyperlysinemia

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(7)
E72.0

Disorders of amino-acid transport

E72.1

Disorders of sulfur-bearing amino-acid metabolism

E72.2

Disorders of urea cycle metabolism

E72.4

Disorders of ornithine metabolism

BillableE72.5

Disorders of glycine metabolism

E72.8

Other specified disorders of amino-acid metabolism

E72.9

Disorder of amino-acid metabolism, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

5C50.4Disorders of lysine or hydroxylysine metabolismequivalentPrimary
Also Known As / Clinical Terms(230)

SNOMED CT

UMLS

Clinical Terms

  • 2-aminoadipic 2-oxoadipic aciduria
  • Lysinuric protein intolerance, type 2
  • Deficiency, Lysine:Alpha-Ketoglutarate Reductase
  • 2-Ketoadipic acidaemia
  • Hyperlysinemias, Familial
  • Dystonia due to glutaric acidemia
  • L-2-HGA
  • Lysine and hydroxylysine metabolism disorder
  • Glutaric acidaemia type 1
  • Congenital enchondromatosis
  • Hyperammonaemia
  • Deficiency of lysine racemase
  • Glutaric aciduria (disorder)
  • Reductase Deficiencies, Lysine:Alpha-Ketoglutarate
  • Periodic hyperlysinaemia
  • Lysine:Alpha Ketoglutarate Reductase Deficiency
  • Hyperlysinemia
  • glutaric aciduria
  • D-2-hydroxyglutaric aciduria
  • L-2-hydroxyglutaric aciduria
  • Persistent hyperlysinaemia
  • Glutaric acidemia type 1
  • GA I
  • 2-hydroxyglutaric aciduria
  • L-2(OH) glutaric aciduria
  • Hyperlysinemia, Familial
  • Saccharopinuria
  • 2-Ketoadipic acidemia
  • Deficiency, L-Lysine:NAD-Oxido-Reductase
  • Persistent hyperlysinemia
  • Glutaric acidemia type I
  • Disorder of lysine and hydroxylysine metabolism
  • Hyperammonemia
  • Deficiencies, Lysine:Alpha-Ketoglutarate Reductase
  • Glutaric aciduria I
  • Glutarate aciduria
  • L Lysine:NAD Oxido Reductase Deficiency
  • Lysine intolerance
  • Lysine:Alpha-Ketoglutarate Reductase Deficiencies
  • Glutaric aciduria 1
  • Periodic hyperlysinemia
  • Inborn error of amino acid metabolism
  • Ollier's disease
  • GA I - glutaric aciduria type 1
  • Disorder of lysine and hydroxylysine metabolism (disorder)
  • GCDH-gene related glutaryl-coenzyme A dehydrogenase deficiency
  • Familial Hyperlysinemias
  • hyperlysinemias
  • Hyperlysinuria with hyperammonemia
  • glutaric aciduria type i
  • Dyschondroplasia
  • Persistent hyperlysinaemia without hyperammonaemia
  • Increased glutarate level in urine
  • Disorder of lysine AND/OR hydroxylysine metabolism (disorder)
  • Periodic hyperlysinaemia with hyperammonaemia
  • Reductase Deficiency, Lysine:Alpha-Ketoglutarate
  • GLUTARIC ACIDEMIA I
  • glutaric aciduria type 1
  • Glutaryl-coenzyme A dehydrogenase deficiency
  • GA1
  • Congenital lysinuria
  • aciduria glutaric
  • L-2-hydroxy-glutaric aciduria
  • L-Lysine:NAD-Oxido-Reductase Deficiency
  • Seizures and intellectual disability due to hydroxylysinuria syndrome
  • D-2(OH) glutaric aciduria
  • Periodic hyperlysinemia with hyperammonemia
  • Glutaryl-CoA dehydrogenase deficiency
  • Glutaric acidemia 1
  • Glutaryl-coenzyme A dehydrogenase deficiency (disorder)
  • Lysinuric protein intolerance, type 1
  • Familial Hyperlysinemia
  • Alpha-aminoadipic semialdehyde deficiency
  • Alpha-aminoadipic aciduria
  • Glutaric aciduria NOS
  • Dibasic aminoaciduria - type I
  • Glutaric acidaemia type I
  • Hyperlysinemia (disorder)
  • Hyperaminoaciduria
  • Hyperlysinuria with hyperammonaemia
  • Enchondromatosis
  • Multiple enchondromata
  • Deficiencies, L-Lysine:NAD-Oxido-Reductase
  • Lysinuric protein intolerance
  • Ollier disease
  • Persistent hyperlysinemia without hyperammonemia
  • Seizures and intellectual disability due to hydroxylysinuria
  • Saccharopine dehydrogenase deficiency
  • Hyperdibasic aminoaciduria
  • Glutaric aciduria (type I)
  • Hydroxylysinemia
  • L-Lysine:NAD-Oxido-Reductase Deficiencies
  • Hyperlysinaemia
  • Glutaricaciduria
  • Dystonia due to glutaric acidaemia
  • Disorder of lysine AND/OR hydroxylysine metabolism
  • Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria
  • LPI - Lysinuric protein intolerance
  • Dibasic aminoaciduria - type II
  • Lysine:Alpha-Ketoglutarate Reductase Deficiency
  • Hydroxylysine present in blood
  • Elevated blood lysine
Frequently Asked Questions
What is the ICD-10 code for disorders of lysine and hydroxylysine metabolism?

The ICD-10-CM code for disorders of lysine and hydroxylysine metabolism is E72.3. The full clinical description is "Disorders of lysine and hydroxylysine metabolism". E72.3 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E72.3 mean?

ICD-10-CM code E72.3 represents “Disorders of lysine and hydroxylysine metabolism”. 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 E72.3 a billable code?

Yes, E72.3 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E72.3 in?

E72.3 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E72.3?

E72.3 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 12 more.

What SNOMED CT codes does E72.3 map to?

E72.3 maps to 25 SNOMED CT concepts: 237931009, 782918002, 698870008, 58558003, 268274005, and 20 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E72.3?

E72.3 is linked to 5 UMLS Concept Unique Identifiers: C0268553, C0268552, C0268595, C0268594, C1399910. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E72.3 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorders of lysine and hydroxylysine metabolism 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 E72.3?

E72.3 maps to the ICD-11 code: 5C50.4 (Disorders of lysine or hydroxylysine metabolism).

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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.