E70.29
BillableOther disorders of tyrosine metabolism
Other disorders of tyrosine metabolism
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)
- 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)
- transitory tyrosinemia of newborn (P74.5)
Excludes 2
Conditions not included here, but the patient may have both
- Ehlers-Danlos syndromes (Q79.6-)
Also Known As / Clinical Terms
SNOMED CT
- Ochronotic arthritis39838007
- Ochronotic arthropathy39838007
- Woolf syndrome74320008
- Woolf's syndrome74320008
- Tyrosinuria123967008
- Deficiency of quinate dehydrogenase124112004
- Deficiency of gentisate 1,2-dioxygenase124206001
- Deficiency of gentisate l,2-dioxygenase124206001
- Deficiency of gentisate oxygenase124206001
- Deficiency of tyrosine decarboxylase124599002
- Deficiency of maleylacetoacetate isomerase124664006
- GSTZ1-gene related deficiency of maleylacetoacetate isomerase124664006
- Deficiency of tyrosine-tRNA ligase124688008
- Deficiency of tyrosine-transfer ribonucleic acid ligase124688008
- Deficiency of tyrosyl-tRNA synthetase124688008
- Degenerative polyarthritis225655006
- Disorder of catecholamine synthesis237921002
- Dopamine beta-hydroxylase deficiency237923004
- Alkaptonuria360378009
- Deficiency of homogentisate 1,2-dioxygenase360378009
- Deficiency of homogentisate oxygenase360378009
- Deficiency of homogentisicase360378009
- HGD-gene related homogentisate 1,2-dioxygenase deficiency360378009
- Hereditary ochronosis360378009
- Homogentisate 1,2-dioxygenase deficiency360378009
- Homogentisic acid oxidase deficiency360378009
- Homogentisicaciduria360378009
- Hepatic tyrosine aminotransferase deficiency360410009
- Non-melanin pigmentation caused by exogenous substance402620009
- Exogenous ochronosis410041002
- Alcaptonuric ochronosis410042009
- Alkaptonuric ochronosis410042009
- Ochronosis410042009
- Ochronosis due to alkaptonuria410042009
- Ochronosis due to homogentisate 1,2-dioxygenase deficiency410042009
- Pigmentation due to alkaptonuria410042009
- 4-Hydroxyphenylpyruvate dioxygenase deficiency413356003
- 4-Hydroxyphenylpyruvate hydroxylase deficiency413356003
- Arthritis due to alkaptonuria431011000124103
- Arthritis due to homogentisate 1,2-dioxygenase deficiency431011000124103
UMLS
- AKUC0002066
- ALKAPTONURIAC0002066
- AlcaptonuriaC0002066
- AlcaptonuriasC0002066
- AlkaptonuriaC0002066
- Black urine diseaseC0002066
- Deficiency of homogentisate 1,2-dioxygenaseC0002066
- Deficiency of homogentisate oxygenaseC0002066
- Deficiency of homogentisicaseC0002066
- HGD-gene related homogentisate 1,2-dioxygenase deficiencyC0002066
- HOMOGENTISIC ACID OXIDASE DEFICIENCYC0002066
- Homogentisate 1,2-dioxygenase deficiencyC0002066
- Homogentisate 1,2-dioxygenase deficiency (disorder)C0002066
- Homogentisic Acid Oxidase DeficiencyC0002066
- Homogentisic AciduraC0002066
- Homogentisic acid oxidase deficiencyC0002066
- Homogentisic aciduraC0002066
- HomogentisicaciduriaC0002066
- alcaptonuriaC0002066
- alkaptonuriaC0002066
- OchronosesC0028817
- OchronosisC0028817
- ochronosesC0028817
- ochronosisC0028817
- Other disorders of tyrosine metabolismC2874228
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.
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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.