ICD-10 Code E03.0: Congenital hypothyroidism with diffuse goiter
What is this code?
ICD-10 codes are diagnosis classification codes used in healthcare records, reporting, coding workflows, and billing support. This code sits within the broader ICD-10 area for Endocrine, nutritional and metabolic diseases (E00-E89).
šClinical overview
This ICD-10 code is commonly used when documentation describes hypothyroidism or another closely related thyroid-hormone deficiency pattern in the E03 family. The most accurate code depends on whether the record identifies congenital, drug-induced, postinfectious, atrophic, myxedema-coma, other specified, or unspecified hypothyroidism.
When is it used?
- May be used when a clinician documents congenital hypothyroidism with diffuse goiter in a patient's medical record.
- May appear in hospital records, claims, referrals, and clinical documentation.
- This code can be used as a clinically usable diagnosis entry in standardized coding workflows.
What it does not mean
- A code alone does not explain severity, treatment plan, or outcome.
- A medical code should not be treated as a substitute for a doctor's diagnosis or advice.
š©ŗClinical context
- Primary-care, endocrinology, inpatient, and utilization-review workflows where thyroid-hormone deficiency, thyroid replacement follow-up, or severe decompensated hypothyroid illness is part of the assessment.
- Coding workflows where the chart identifies congenital status, medication or exogenous cause, infection-related onset, myxedema-coma severity, or another specific hypothyroid pattern that changes final code specificity.
- Common related testing on this page includes TSH, Free T4, Anti-thyroid peroxidase antibody.
- Evaluation often includes TSH and free-thyroxine review, symptom assessment for fatigue, cold intolerance, constipation, weight change, or altered mental status, and thyroid-replacement or endocrine follow-up planning.
- Documentation usually becomes more specific when the chart identifies congenital versus acquired disease, drug-related or postinfectious cause, thyroid atrophy, myxedema-coma severity, or another specified hypothyroid pattern.
- Specialist context already linked on this page includes Endocrinologist, General Physician.
šKey distinctions
- This ICD-10 family captures hypothyroidism and closely related thyroid-hormone deficiency states rather than thyroiditis, hyperthyroidism, or non-thyroid endocrine disorders.
- Cause and severity detail, such as congenital pattern, exogenous cause, postinfectious state, thyroid atrophy, myxedema coma, other specified form, or unspecified disease, drives final code specificity inside this family.
- Congenital hypothyroidism with diffuse goiter is coded separately from congenital hypothyroidism without goiter and from acquired hypothyroid patterns.
- Documentation that describes hypothyroidism is coded differently from thyroiditis, thyrotoxicosis, hyperparathyroidism, or other endocrine disorders without documented thyroid-hormone deficiency.
- transitory congenital goiter with normal function (P72.0)
Code hierarchy
Official coding notes
- Congenital parenchymatous goiter (nontoxic)
- Congenital goiter (nontoxic) NOS
- transitory congenital goiter with normal function (P72.0)
Where you may see this code
You may see this code in hospital records, discharge summaries, insurance claims, encounter documentation, referrals, or other healthcare billing and coding records.
Related specialists
Related tests
Related codes
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Coverage-related procedures and services
Mapped diagnoses and classifications
Coding guidelines
Compatibility
Common synonyms
Frequently asked questions
About this content
This page is prepared by HealthAssure's clinical team using official coding standards from ICD-10. AI tools assist with drafting explanations, which are then reviewed and verified by healthcare professionals for accuracy. This content is for informational purposes and does not replace professional medical advice. Meet our team.