E00.1
BillableCongenital iodine-deficiency syndrome, myxedematous type
Congenital iodine-deficiency syndrome, myxedematous type
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Endemic hypothyroid cretinism
- Endemic cretinism, myxedematous type
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Use Additional Code
Additional codes that should follow this code
Related Codes(3)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(71)
SNOMED CT
- Myxedema43153006
- Myxoedema43153006
- Congenital myxedema64491003
- Congenital myxoedema64491003
- Myxedematous form of cretinism64491003
- Myxoedematous form of cretinism64491003
- Endemic cretinism75065003
- Congenital goiter217710005
- Congenital goitre217710005
- Congenital hypothyroidism not due to iodine deficiency217710005
- Congenital iodine deficiency syndrome217710005
- Cretinism217710005
- Fetal iodine deficiency syndrome217710005
- Foetal iodine deficiency syndrome217710005
- Infantile hypothyroidism217710005
- Endemic congenital iodine deficiency syndrome of myxedematous type440092001
- Endemic congenital iodine deficiency syndrome of myxoedematous type440092001
- Myxedematous form of endemic cretinism440092001
- Myxoedematous form of endemic cretinism440092001
UMLS
- Congenital Iodine Deficiency Syndrome, Myxedematous TypeC2584703
- Congenital iodine-deficiency syndrome, myxedematous typeC2584703
- Endemic congenital iodine deficiency syndrome of myxedematous typeC2584703
- Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)C2584703
- Endemic congenital iodine deficiency syndrome of myxoedematous typeC2584703
- Endemic cretinism, myxedematous typeC2584703
- Myxedematous form of cretinismC2584703
- Myxedematous form of cretinism (disorder)C2584703
- Myxedematous form of endemic cretinismC2584703
- Myxoedematous form of cretinismC2584703
- Myxoedematous form of endemic cretinismC2584703
- Cretinism, EndemicC0342200
- ENDEMIC CRETINISMC0342200
- Endemic CretinismC0342200
- Endemic cretinismC0342200
- Endemic cretinism (disorder)C0342200
- Endemic hypothyroid cretinismC0342200
- FETAL IODINE DEFICIENCY DISORDERC0342200
- FIDDC0342200
- Fetal Iodine Deficiency DisorderC0342200
- cretinismC0342200
- endemic cretinismC0342200
- goitrous cretinismC0342200
Clinical Terms
- FETAL IODINE DEFICIENCY DISORDER
- Myxedematous form of cretinism
- ENDEMIC CRETINISM
- Cretinism
- Endemic cretinism (disorder)
- Myxedema
- Endemic congenital iodine deficiency syndrome of myxoedematous type
- Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)
- Infantile hypothyroidism
- Myxedematous form of endemic cretinism
- Congenital myxoedema
- Fetal iodine deficiency syndrome
- Cretinism, Endemic
- Congenital goitre
- Endemic hypothyroid cretinism
- Foetal iodine deficiency syndrome
- Myxoedematous form of endemic cretinism
- Myxedematous form of cretinism (disorder)
- Congenital Iodine Deficiency Syndrome, Myxedematous Type
- Myxoedematous form of cretinism
- Endemic cretinism, myxedematous type
- Congenital myxedema
- Congenital hypothyroidism not due to iodine deficiency
- goitrous cretinism
- FIDD
- Myxoedema
- Endemic congenital iodine deficiency syndrome of myxedematous type
- Congenital goiter
- Congenital iodine deficiency syndrome
Frequently Asked Questions
What is the ICD-10 code for congenital iodine-deficiency syndrome, myxedematous type?
The ICD-10-CM code for congenital iodine-deficiency syndrome, myxedematous type is E00.1. The full clinical description is "Congenital iodine-deficiency syndrome, myxedematous type". E00.1 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E00.1 mean?
ICD-10-CM code E00.1 represents “Congenital iodine-deficiency syndrome, myxedematous 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 E00.1 a billable code?
Yes, E00.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E00.1 in?
E00.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E00.1?
E00.1 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 E00.1?
Yes, when using E00.1, also report: code (F70-F79) to identify associated intellectual disabilities..
What SNOMED CT codes does E00.1 map to?
E00.1 maps to 5 SNOMED CT concepts: 217710005, 64491003, 440092001, 75065003, 43153006. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E00.1?
E00.1 is linked to 2 UMLS Concept Unique Identifiers: C2584703, C0342200. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E00.1 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital iodine-deficiency syndrome, myxedematous 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 E00.1?
E00.1 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.