AutoICD API

E00.2

Billable

Congenital iodine-deficiency syndrome, mixed type

Congenital iodine-deficiency syndrome, mixed type

Status

Billable / Specific

Block

E00-E07

Parent Code

E00

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Endemic cretinism, mixed type

Use Additional Code

Additional codes that should follow this code

Related Codes(3)
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

Also Known As / Clinical Terms(55)

Clinical Terms

  • Endemic cretinism of mixed type
  • Myxedematous form of cretinism
  • Cretinism
  • Congenital Iodine Deficiency Syndrome, Mixed Type
  • Myxedema
  • Endemic congenital iodine deficiency syndrome of myxoedematous type
  • Infantile hypothyroidism
  • Myxedematous form of endemic cretinism
  • Congenital myxoedema
  • Fetal iodine deficiency syndrome
  • Endemic cretinism, mixed type
  • Congenital goitre
  • Foetal iodine deficiency syndrome
  • Myxoedematous form of endemic cretinism
  • Myxoedematous form of cretinism
  • Congenital myxedema
  • Congenital iodine deficiency syndrome of mixed type (disorder)
  • Endemic cretinism of neurological type
  • Congenital hypothyroidism not due to iodine deficiency
  • Endemic cretinism
  • Myxoedema
  • Endemic congenital iodine deficiency syndrome of myxedematous type
  • Congenital iodine deficiency syndrome of neurological type
  • Congenital goiter
  • Congenital iodine deficiency syndrome of mixed type
  • Congenital iodine deficiency syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital iodine-deficiency syndrome, mixed type?

The ICD-10-CM code for congenital iodine-deficiency syndrome, mixed type is E00.2. The full clinical description is "Congenital iodine-deficiency syndrome, mixed type". E00.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E00.2 mean?

ICD-10-CM code E00.2 represents “Congenital iodine-deficiency syndrome, mixed type”. 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 E00.2 a billable code?

Yes, E00.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E00.2 in?

E00.2 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E00.2?

E00.2 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); subclinical iodine-deficiency hypothyroidism (E02).

Are additional codes required with E00.2?

Yes, when using E00.2, also report: code (F70-F79) to identify associated intellectual disabilities..

What SNOMED CT codes does E00.2 map to?

E00.2 maps to 7 SNOMED CT concepts: 217710005, 237565000, 237566004, 64491003, 440092001, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E00.2?

E00.2 is linked to 1 UMLS Concept Unique Identifier: C0342202. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E00.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital iodine-deficiency syndrome, mixed type 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 E00.2?

E00.2 maps to the ICD-11 code: 5A00.04 (Congenital hypothyroidism due to iodine deficiency).

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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.