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ICD-10-CM Codes
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E00-E89
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E00-E07
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E03-
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2023 ICD-10-CM Diagnosis Code E03.1
2023 ICD-10-CM Diagnosis Code E03.1
Congenital hypothyroidism without goiter
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- E03.1 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2023 edition of ICD-10-CM E03.1 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E03.1 - other international versions of ICD-10 E03.1 may differ.
Applicable To- Aplasia of thyroid (with myxedema)
- Congenital atrophy of thyroid
- Congenital hypothyroidism NOS
The following code(s) above
E03.1 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
- Applicable To annotations, or
- Code Also annotations, or
- Code First annotations, or
- Excludes1 annotations, or
- Excludes2 annotations, or
- Includes annotations, or
- Note annotations, or
- Use Additional annotations
that may be applicable to
E03.1:
Approximate Synonyms
- Congenital hypothyroidism
- Hypothyroidism, congenital
Clinical Information
- A condition in infancy or early childhood due to an in-utero deficiency of thyroid hormones that can be caused by genetic or environmental factors, such as thyroid dysgenesis or hypothyroidism in infants of mothers treated with thiouracil during pregnancy. Endemic cretinism is the result of iodine deficiency. Clinical symptoms include severe mental retardation, impaired skeletal development, short stature, and myxedema.
- A deficiency of thyroid hormone present at birth. The etiology can be genetic or environmental, or a combination of both; treatment is based on severity and causality.
- Condition due to congenital lack of thyroid hormone, marked by arrested physical and mental development, dystrophy of the bones and soft parts, and lowered basal metabolism; it is the congenital form of thyroid deficiency, while myxedema is the acquired form.
ICD-10-CM E03.1 is grouped within Diagnostic Related Group(s) (MS-DRG v40.0):
- 643 Endocrine disorders with mcc
- 644 Endocrine disorders with cc
- 645 Endocrine disorders without cc/mcc
Convert E03.1 to ICD-9-CM
Code 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
Code annotations containing back-references to E03.1:
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Type 1 Excludes: P72, E03.4, Q89.2
ICD-10-CM Diagnosis Code P72
Other transitory neonatal endocrine disorders
2016 2017 2018 2019 2020 2021 2022 2023 Non-Billable/Non-Specific Code
Type 1 Excludes- congenital hypothyroidism with or without goiter (E03.0-E03.1)
- dyshormogenetic goiter (E07.1)
- Pendred's syndrome (E07.1)
ICD-10-CM Diagnosis Code E03.4
Atrophy of thyroid (acquired)
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Type 1 Excludes- congenital atrophy of thyroid (E03.1)
ICD-10-CM Diagnosis Code Q89.2
Congenital malformations of other endocrine glands
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code POA Exempt
Applicable To- Congenital malformation of parathyroid or thyroid gland
- Persistent thyroglossal duct
- Thyroglossal cyst
Type 1 Excludes- congenital goiter (E03.0)
- congenital hypothyroidism (E03.1)
- Absence (of) (organ or part) (complete or partial)
- thyroid (gland) (acquired) E89.0
ICD-10-CM Diagnosis Code E89.0
Postprocedural hypothyroidism
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Applicable To- Postirradiation hypothyroidism
- Postsurgical hypothyroidism
- Agenesis
- Aplasia - see also Agenesis
- thyroid E03.1 (congenital) (with myxedema)
- Athyrea (acquired) - see also Hypothyroidism
- Atrophy, atrophic (of)
- thyroid (gland) (acquired) E03.4
ICD-10-CM Diagnosis Code E03.4
Atrophy of thyroid (acquired)
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
Type 1 Excludes- congenital atrophy of thyroid (E03.1)
- with cretinism E03.1
- congenital E03.1 (with myxedema)
- Hypoplasia, hypoplastic
- Hypothyroidism (acquired) E03.9
ICD-10-CM Diagnosis Code E03.9
Hypothyroidism, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Insufficiency, insufficient
- thyroid (gland) (acquired) E03.9
ICD-10-CM Diagnosis Code E03.9
Hypothyroidism, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- Jaundice (yellow) R17
ICD-10-CM Diagnosis Code R17
Unspecified jaundice
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code
- newborn P59.9
ICD-10-CM Diagnosis Code P59.9
Neonatal jaundice, unspecified
2016 2017 2018 2019 2020 2021 2022 2023 Billable/Specific Code Code on Newborn Record
Applicable To- Neonatal physiological jaundice (intense)(prolonged) NOS
- Subthyroidism (acquired) - see also Hypothyroidism
ICD-10-CM Codes Adjacent To E03.1
E00.2 Congenital iodine-deficiency syndrome, mixed type
E00.9 Congenital iodine-deficiency syndrome, unspecified
E01 Iodine-deficiency related thyroid disorders and allied conditions
E01.0 Iodine-deficiency related diffuse (endemic) goiter
E01.1 Iodine-deficiency related multinodular (endemic) goiter
E01.2 Iodine-deficiency related (endemic) goiter, unspecified
E01.8 Other iodine-deficiency related thyroid disorders and allied conditions
E02 Subclinical iodine-deficiency hypothyroidism
E03.0 Congenital hypothyroidism with diffuse goiter
E03.1
Congenital hypothyroidism without goiter
E03.2 Hypothyroidism due to medicaments and other exogenous substances
E03.3 Postinfectious hypothyroidism
E03.4 Atrophy of thyroid (acquired)
E03.8 Other specified hypothyroidism
E03.9 Hypothyroidism, unspecified
E04 Other nontoxic goiter
E04.0 Nontoxic diffuse goiter
E04.1 Nontoxic single thyroid nodule
E04.2 Nontoxic multinodular goiter
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.