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E70.29

Billable

Other disorders of tyrosine metabolism

Other disorders of tyrosine metabolism

Status

Billable / Specific

Block

E70-E88

Parent Code

E70.2

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Alkaptonuria
  • Ochronosis

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(2)
E70.20

Disorder of tyrosine metabolism, unspecified

BillableE70.21

Tyrosinemia

Billable
Also Known As / Clinical Terms(112)

SNOMED CT

UMLS

Clinical Terms

  • HOMOGENTISIC ACID OXIDASE DEFICIENCY
  • Ochronotic arthropathy
  • Deficiency of homogentisate 1,2-dioxygenase
  • Deficiency of tyrosine decarboxylase
  • Alcaptonuria
  • Arthritis due to homogentisate 1,2-dioxygenase deficiency
  • Deficiency of gentisate l,2-dioxygenase
  • Deficiency of quinate dehydrogenase
  • Disorder of catecholamine synthesis
  • Alkaptonuric ochronosis
  • Tyrosinuria
  • Black urine disease
  • alkaptonuria
  • Ochronoses
  • Deficiency of maleylacetoacetate isomerase
  • GSTZ1-gene related deficiency of maleylacetoacetate isomerase
  • Ochronosis
  • Arthritis due to alkaptonuria
  • Deficiency of homogentisate oxygenase
  • Deficiency of homogentisicase
  • Non-melanin pigmentation caused by exogenous substance
  • Degenerative polyarthritis
  • Homogentisic acidura
  • Deficiency of tyrosine-tRNA ligase
  • Ochronosis due to alkaptonuria
  • Hereditary ochronosis
  • AKU
  • 4-Hydroxyphenylpyruvate hydroxylase deficiency
  • Exogenous ochronosis
  • Hepatic tyrosine aminotransferase deficiency
  • Deficiency of gentisate 1,2-dioxygenase
  • Woolf syndrome
  • Ochronotic arthritis
  • Pigmentation due to alkaptonuria
  • Homogentisicaciduria
  • Deficiency of gentisate oxygenase
  • Dopamine beta-hydroxylase deficiency
  • Alcaptonurias
  • Homogentisate 1,2-dioxygenase deficiency
  • Homogentisate 1,2-dioxygenase deficiency (disorder)
  • Deficiency of tyrosine-transfer ribonucleic acid ligase
  • Deficiency of tyrosyl-tRNA synthetase
  • Alcaptonuric ochronosis
  • HGD-gene related homogentisate 1,2-dioxygenase deficiency
  • 4-Hydroxyphenylpyruvate dioxygenase deficiency
  • Ochronosis due to homogentisate 1,2-dioxygenase deficiency
  • Woolf's syndrome
Frequently Asked Questions
What is the ICD-10 code for other disorders of tyrosine metabolism?

The ICD-10-CM code for other disorders of tyrosine metabolism is E70.29. The full clinical description is "Other disorders of tyrosine metabolism". E70.29 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E70.29 mean?

ICD-10-CM code E70.29 represents “Other disorders of tyrosine 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 E70.29 a billable code?

Yes, E70.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E70.29 in?

E70.29 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E70.29?

E70.29 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 4 more.

What SNOMED CT codes does E70.29 map to?

E70.29 maps to 18 SNOMED CT concepts: 413356003, 410042009, 360378009, 431011000124103, 124206001, and 13 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E70.29?

E70.29 is linked to 3 UMLS Concept Unique Identifiers: C0002066, C0028817, C2874228. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E70.29 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of tyrosine 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 E70.29?

There is no direct ICD-11 mapping available for E70.29 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.