Congenital iodine-deficiency syndrome, myxedematous type
- E00.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2025 edition of ICD-10-CM E00.1 became effective on October 1, 2024.
- This is the American ICD-10-CM version of E00.1 – other international versions of ICD-10 E00.1 may differ.
Applicable To
- Endemic hypothyroid cretinism
- Endemic cretinism, myxedematous type
The following code(s) above E00.1 contain annotation back-references
that may be applicable to E00.1:
Approximate Synonyms
- Congenital iodine deficiency syndrome, myxedematous ty
- Endemic congenital iodine deficiency syndrome of myxedematous type
Clinical Information
- Severely reduced physical and mental growth associated with pyramidal and extrapyramidal signs and symptoms, due to dietary iodine deficiency.
ICD-10-CM E00.1 is grouped within Diagnostic Related Group(s) (MS-DRG v42.0):
- 643 Endocrine disorders with mcc
- 644 Endocrine disorders with cc
- 645 Endocrine disorders without cc/mcc
Convert E00.1 to ICD-9-CMCode History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2017 (effective 10/1/2016): No change
- 2018 (effective 10/1/2017): No change
- 2019 (effective 10/1/2018): No change
- 2020 (effective 10/1/2019): No change
- 2021 (effective 10/1/2020): No change
- 2022 (effective 10/1/2021): No change
- 2023 (effective 10/1/2022): No change
- 2024 (effective 10/1/2023): No change
- 2025 (effective 10/1/2024): No change
Code annotations containing back-references to E00.1:
- Code First: G13.2
Diagnosis Index entries containing back-references to E00.1:
- Cretin, cretinism (congenital) (endemic) (nongoitrous) (sporadic) E00.9
- type
- hypothyroid E00.1
- myxedematous E00.1
- type
- Myxedema (adult) (idiocy) (infantile) (juvenile) E03.9 – see also Hypothyroidism
- congenital E00.1
- Syndrome – see also Disease
- iodine-deficiency, congenitalE00.9
- type
- myxedematous E00.1
- type
- iodine-deficiency, congenitalE00.9