AutoICD API

E70.321

Billable

Tyrosinase positive oculocutaneous albinism

Tyrosinase positive oculocutaneous albinism

Status

Billable / Specific

Block

E70-E88

Parent Code

E70.32

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Albinism II
  • Oculocutaneous albinism ty-pos

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)
  • Chediak-Higashi syndrome (E70.330)
  • Hermansky-Pudlak syndrome (E70.331)

Excludes 2

Conditions not included here, but the patient may have both

  • Ehlers-Danlos syndromes (Q79.6-)

Also Known As / Clinical Terms

SNOMED CT

UMLS

Frequently Asked Questions

What is the ICD-10 code for tyrosinase positive oculocutaneous albinism?

The ICD-10-CM code for tyrosinase positive oculocutaneous albinism is E70.321. The full clinical description is "Tyrosinase positive oculocutaneous albinism". E70.321 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E70.321 mean?

ICD-10-CM code E70.321 represents "Tyrosinase positive oculocutaneous albinism". 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 E70.321 a billable code?

Yes, E70.321 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E70.321 in?

E70.321 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E70.321?

E70.321 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 5 more.

What SNOMED CT codes does E70.321 map to?

E70.321 maps to 3 SNOMED CT concepts: 26336006, 11160000, 63450009. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E70.321?

E70.321 is linked to 1 UMLS Concept Unique Identifier: C0268495. 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.