E00.1
Billable codeCongenital iodine-deficiency syndrome, myxedematous type
The ICD-10 code for congenital iodine-deficiency syndrome, myxedematous type is E00.1.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- Endemic hypothyroid cretinism
- Endemic cretinism, myxedematous type
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- E00.0Congenital iodine-deficiency syndrome, neurological type
- E00.2Congenital iodine-deficiency syndrome, mixed type
- E00.9Congenital iodine-deficiency syndrome, unspecified
- E00.1Congenital iodine-deficiency syndrome, myxedematous type
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 243Approximate match
Associated MS-DRGs
E00.1 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.