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
- code (F70-F79) to identify associated intellectual disabilities.
Also Known As / Clinical Terms
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
Frequently Asked Questions
What is ICD-10 code E00.1?
ICD-10-CM code E00.1 represents "Congenital iodine-deficiency syndrome, myxedematous type". It 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 you should also code: 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.
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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.