E72.3
BillableDisorders of lysine and hydroxylysine metabolism
Disorders of lysine and hydroxylysine metabolism
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)
- 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.-)
- glutaric aciduria type II (E71.313)
- Refsum's disease (G60.1)
- Zellweger syndrome (E71.510)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Hyperammonaemia9360008
- Hyperammonemia9360008
- Glutaric aciduria28987007
- Hyperaminoaciduria42930003
- Inborn error of amino acid metabolism42930003
- Dibasic aminoaciduria - type I50056009
- Lysinuric protein intolerance, type 150056009
- Alpha-aminoadipic semialdehyde deficiency58558003
- Hyperlysinaemia58558003
- Hyperlysinemia58558003
- Saccharopine dehydrogenase deficiency58558003
- Persistent hyperlysinaemia66002008
- Persistent hyperlysinaemia without hyperammonaemia66002008
- Persistent hyperlysinemia66002008
- Persistent hyperlysinemia without hyperammonemia66002008
- Dibasic aminoaciduria - type II71751002
- Lysinuric protein intolerance, type 271751002
- Disorder of lysine AND/OR hydroxylysine metabolism77402005
- Saccharopinuria111397004
- Deficiency of lysine racemase124658004
- Disorder of lysine and hydroxylysine metabolism237929000
- Lysine and hydroxylysine metabolism disorder237929000
- 2-Ketoadipic acidaemia237931009
- 2-Ketoadipic acidemia237931009
- D-2(OH) glutaric aciduria237960000
- D-2-hydroxyglutaric aciduria237960000
- L-2(OH) glutaric aciduria237961001
- L-2-HGA237961001
- L-2-hydroxy-glutaric aciduria237961001
- L-2-hydroxyglutaric aciduria237961001
- Congenital enchondromatosis268274005
- Dyschondroplasia268274005
- Enchondromatosis268274005
- Multiple enchondromata268274005
- Ollier disease268274005
- Ollier's disease268274005
- Congenital lysinuria303852004
- Hyperdibasic aminoaciduria303852004
- LPI - Lysinuric protein intolerance303852004
- Lysinuric protein intolerance303852004
- Lysine intolerance340519003
- Periodic hyperlysinaemia341536001
- Periodic hyperlysinemia341536001
- Hyperlysinuria with hyperammonaemia342553006
- Hyperlysinuria with hyperammonemia342553006
- Periodic hyperlysinaemia with hyperammonaemia342553006
- Periodic hyperlysinemia with hyperammonemia342553006
- GA I - glutaric aciduria type 1360416003
- GCDH-gene related glutaryl-coenzyme A dehydrogenase deficiency360416003
- Glutaric acidaemia type 1360416003
- Glutaric acidemia type 1360416003
- Glutaric aciduria type 1360416003
- Glutaryl-CoA dehydrogenase deficiency360416003
- Glutaryl-coenzyme A dehydrogenase deficiency360416003
- 2-hydroxyglutaric aciduria698870008
- Seizures and intellectual disability due to hydroxylysinuria723994004
- Seizures and intellectual disability due to hydroxylysinuria syndrome723994004
- Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria724146008
- 2-aminoadipic 2-oxoadipic aciduria782918002
- Alpha-aminoadipic aciduria782918002
- Dystonia due to glutaric acidaemia1260378000
- Dystonia due to glutaric acidemia1260378000
UMLS
- Deficiencies, L-Lysine:NAD-Oxido-ReductaseC0268553
- Deficiencies, Lysine:Alpha-Ketoglutarate ReductaseC0268553
- Deficiency, L-Lysine:NAD-Oxido-ReductaseC0268553
- Deficiency, Lysine:Alpha-Ketoglutarate ReductaseC0268553
- Elevated blood lysineC0268553
- Familial HyperlysinemiaC0268553
- Familial HyperlysinemiasC0268553
- Familial hyperlysinemiaC0268553
- HyperlysinaemiaC0268553
- HyperlysinemiaC0268553
- Hyperlysinemia (disorder)C0268553
- Hyperlysinemia, FamilialC0268553
- HyperlysinemiasC0268553
- Hyperlysinemias, FamilialC0268553
- L Lysine:NAD Oxido Reductase DeficiencyC0268553
- L-Lysine:NAD-Oxido-Reductase DeficienciesC0268553
- L-Lysine:NAD-Oxido-Reductase DeficiencyC0268553
- Lysine:Alpha Ketoglutarate Reductase DeficiencyC0268553
- Lysine:Alpha-Ketoglutarate Reductase DeficienciesC0268553
- Lysine:Alpha-Ketoglutarate Reductase DeficiencyC0268553
- Reductase Deficiencies, Lysine:Alpha-KetoglutarateC0268553
- Reductase Deficiency, Lysine:Alpha-KetoglutarateC0268553
- hyperlysinemiaC0268553
- hyperlysinemiasC0268553
- Disorder of lysine AND/OR hydroxylysine metabolismC0268552
- Disorder of lysine AND/OR hydroxylysine metabolism (disorder)C0268552
- Disorder of lysine and hydroxylysine metabolismC0268552
- Disorder of lysine and hydroxylysine metabolism (disorder)C0268552
- Disorders of lysine and hydroxylysine metabolismC0268552
- Lysine and hydroxylysine metabolism disorderC0268552
- GA IC0268595
- GA I - glutaric aciduria type 1C0268595
- GA1C0268595
- GCDH-gene related glutaryl-coenzyme A dehydrogenase deficiencyC0268595
- GLUTARIC ACIDEMIA IC0268595
- GLUTARIC ACIDURIA IC0268595
- GLUTARYL-CoA DEHYDROGENASE DEFICIENCYC0268595
- Glutaric Acidemia IC0268595
- Glutaric Acidemia Type 1C0268595
- Glutaric Acidemia Type IC0268595
- Glutaric Aciduria IC0268595
- Glutaric acidaemia type 1C0268595
- Glutaric acidaemia type IC0268595
- Glutaric acidemia 1C0268595
- Glutaric acidemia IC0268595
- Glutaric acidemia type 1C0268595
- Glutaric acidemia type IC0268595
- Glutaric aciduria (type I)C0268595
- Glutaric aciduria 1C0268595
- Glutaric aciduria IC0268595
- Glutaric aciduria type 1C0268595
- Glutaryl-CoA dehydrogenase deficiencyC0268595
- Glutaryl-coenzyme A dehydrogenase deficiencyC0268595
- Glutaryl-coenzyme A dehydrogenase deficiency (disorder)C0268595
- glutaric aciduria type 1C0268595
- glutaric aciduria type iC0268595
- Glutarate aciduriaC0268594
- Glutaric aciduriaC0268594
- Glutaric aciduria (disorder)C0268594
- Glutaric aciduria NOSC0268594
- GlutaricaciduriaC0268594
- Increased glutarate level in urineC0268594
- aciduria glutaricC0268594
- glutaric aciduriaC0268594
- Hydroxylysine present in bloodC1399910
- HydroxylysinemiaC1399910
Frequently Asked Questions
What is ICD-10 code E72.3?
ICD-10-CM code E72.3 represents "Disorders of lysine and hydroxylysine metabolism". It 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.
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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.