Congenital iodine-deficiency syndrome, mixed type is a condition resulting from inadequate iodine during fetal development, leading to a spectrum of physical and cognitive impairments. Accurate coding with ICD-10 Code E00.2 is essential for proper diagnosis, documentation, medical billing, and public health reporting, ensuring that affected individuals receive appropriate care and resources.
ICD-10 Code E00.2 represents Congenital iodine-deficiency syndrome, mixed type, characterized by a combination of hypothyroidism and developmental delays due to insufficient iodine during pregnancy. This code should be used in clinical documentation and billing when diagnosing patients with this condition to ensure accurate representation of the patient's health status and facilitate appropriate treatment.
Congenital iodine-deficiency syndrome, mixed type is primarily caused by maternal iodine deficiency during pregnancy, leading to impaired thyroid hormone production in the fetus. This condition can result in severe developmental issues and requires prompt medical attention to mitigate long-term effects.
In SOAP notes, ICD-10 Code E00.2 is utilized to document the diagnosis of Congenital iodine-deficiency syndrome, mixed type, capturing relevant symptoms, assessments, and treatment plans. This code is vital in both acute and chronic care settings to ensure comprehensive patient management.
ICD-10 Code E00.2 connects subjective patient reports and objective clinical findings to a formal diagnosis of Congenital iodine-deficiency syndrome, mixed type. This code is crucial for ensuring continuity of care, supporting billing processes, and meeting EHR documentation standards.
Management of Congenital iodine-deficiency syndrome, mixed type requires urgent intervention to address thyroid hormone deficiencies and associated complications.


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Learn moreICD-10 Code E00.2 is critical in medical billing, particularly in hospital, emergency room, or infectious disease care settings.
| CPT Code | Description |
|---|---|
| 99213 | Established patient office visit, low complexity. |
| 83036 | Thyroid function test (TSH, T4). |
| 99406 | Smoking cessation counseling visit. |
Common Questions About Using ICD-10 Code E00.2 for Congenital iodine-deficiency syndrome, mixed type
What are the main causes of Congenital iodine-deficiency syndrome?
The primary cause of Congenital iodine-deficiency syndrome is maternal iodine deficiency during pregnancy, which leads to inadequate thyroid hormone production in the developing fetus.
How is Congenital iodine-deficiency syndrome diagnosed?
Diagnosis is typically made through clinical evaluation, thyroid function tests, and assessment of developmental milestones in infants and children.
What treatments are available for Congenital iodine-deficiency syndrome?
Treatment primarily involves thyroid hormone replacement therapy, nutritional support, and early intervention programs to address developmental delays.
Is Congenital iodine-deficiency syndrome preventable?
Yes, adequate iodine supplementation during pregnancy can prevent Congenital iodine-deficiency syndrome, highlighting the importance of maternal nutrition.
Clinical Notes
SOAP notes
DAP notes
AI medical notes