Congenital hypothyroidism without goiter is a condition characterized by an underactive thyroid gland present at birth, leading to insufficient production of thyroid hormones. This condition can result from genetic factors or developmental issues affecting the thyroid gland. Accurate coding with ICD-10 Code E03.1 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that patients receive appropriate management and follow-up care.
ICD-10 Code E03.1 represents congenital hypothyroidism without goiter, a condition where the thyroid gland fails to produce adequate hormones from birth, but without the presence of an enlarged thyroid. This code should be used in clinical documentation and billing when diagnosing patients with this specific form of hypothyroidism, ensuring accurate representation of the patient's condition for treatment and reimbursement purposes.
Congenital hypothyroidism without goiter is primarily caused by genetic mutations or developmental anomalies affecting thyroid gland function. If untreated, it can lead to severe developmental delays and metabolic issues. Early diagnosis and intervention are crucial to prevent long-term complications.
ICD-10 Code E03.1 is utilized in SOAP notes to document the patient's symptoms, assessment findings, and treatment plans. It plays a vital role in both acute and chronic care settings, ensuring comprehensive documentation of the patient's condition and facilitating appropriate management.
In SOAP notes, ICD-10 Code E03.1 connects subjective reports of symptoms and objective clinical findings to a formal diagnosis of congenital hypothyroidism without goiter. This ensures continuity of care, supports accurate billing, and meets EHR documentation standards.
Management of congenital hypothyroidism without goiter requires prompt intervention to prevent developmental delays. Treatment typically involves lifelong thyroid hormone replacement therapy.


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Learn moreICD-10 Code E03.1 is critical in medical billing, particularly in hospital, ER, or pediatric care settings.
| CPT Code | Description |
|---|---|
| 84443 | Thyroid stimulating hormone (TSH) test. |
| 84436 | Thyroxine (T4) test. |
| 99213 | Established patient office visit, Level 3. |
Common Questions About Using ICD-10 Code E03.1 for Congenital hypothyroidism without goiter
What are the long-term effects of untreated congenital hypothyroidism?
Untreated congenital hypothyroidism can lead to severe developmental delays, intellectual disability, and growth failure. Early diagnosis and treatment are crucial to prevent these outcomes.
How is congenital hypothyroidism diagnosed?
Congenital hypothyroidism is typically diagnosed through newborn screening tests that measure thyroid hormone levels. Follow-up testing confirms the diagnosis.
Is congenital hypothyroidism hereditary?
Congenital hypothyroidism can be hereditary, often due to genetic mutations affecting thyroid development or function. Family history may increase the risk.
What is the treatment for congenital hypothyroidism?
The primary treatment for congenital hypothyroidism is lifelong thyroid hormone replacement therapy, usually with levothyroxine, to normalize hormone levels and support growth.
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