Infant hypothyroidism
Congenital hypothyroidism due to absence of thyroid gland
Genetic transient congenital hypothyroidism
Hypothyroidism, Congenital
Fetal iodine deficiency syndrome
Congenital goitre
Congenital atrophy of thyroid (disorder)
congenital hypothyroidism
Foetal iodine deficiency syndrome
Congenital thyroid aplasia
Hypothyroidism due to mutation in transcription factor of pituitary development
Congenital hypothyroidism due to maternal intake of antithyroid drug
KMT2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
Hypertrophy of testis
Developmental malformation of branchial arch
Congenital hypothyroidism without goitre
Transient hypothyroidism
Primary hypothyroidism
Hypothyroidism due to TSH receptor mutation
Congenital hypothyroidism due to transplacental passage of maternal TSH (thyroid stimulating hormone)-binding inhibitory antibody
Hypothyroidism congenital
Thyroid hormone resistance syndrome
Cretinism
Choanal atresia
Underactive thyroid gland from birth
Hypothyroidism due to TSHR (thyroid stimulating hormone receptor) mutation
Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency
Congenital thyroid hypoplasia
Congenital central hypothyroidism
TRH (thyrotropin-releasing hormone) resistance syndrome
CONGEN HYPOTHYROIDISM
Familial thyroid dyshormonogenesis
infantile hypothyroidism
Congenital atresia of choana
Congenital hypothyroidism without goiter (disorder)
Congenital hemiagenesis of thyroid
Brain lung thyroid syndrome
Hypoplasia of thyroid
Thyroid hemiagenesis
Congenital hypothyroidism not due to iodine deficiency
IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome
Atresia of posterior nares
Congenital hypothyroidism due to thyroid peroxidase mutation
Congenital goiter
Congenital Thyroid Gland Aplasia
Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome
Atresia of posterior naris
Aplasia of thyroid (with myxedema)
CHT
Congenital atresia of posterior nares
Resistance to TH (thyroid hormone) syndrome
Resistance to thyroid hormone alpha
Congenital hypothyroidism due to thyroglobulin mutation
Idiopathic congenital hypothyroidism
Congenital absence of thyroid gland (disorder)
X-linked central congenital hypothyroidism with late-onset macroorchidism
Degeneration of thyroid
Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome
Congenital atrophy of thyroid
Thyroid degeneration
Transient congenital hypothyroidism due to dual oxidase 2 mutation
Thyroid atrophy
thyroid agenesis
Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody
Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation
Congenital hypothyroidism due to thyroid deiodinase mutation
Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome
Agenesis, Thyroid
Congenital hypothyroidism due to symporter mutation
Neonatal jaundice with congenital hypothyroidism
Congenital absence of thyroid gland
Congenital hypothyroidism due to congenital anomaly of thyroid gland
RTH (resistance to thyroid hormone) syndrome
Resistance to thyroid hormone due to mutation in TRa
Congenital hypothyroidism (disorder)
agenesis thyroid
Central hypothyroidism
Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha
Congenital absence of half of thyroid
Congenital hypothyroidism NOS
Thyroid hormone resistance
X-linked central congenital hypothyroidism with late-onset testicular enlargement
Congenital hypothyroidism due to dual oxidase maturation factor 2
Resistance to thyrotropin-releasing hormone syndrome
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome
Resistance to thyroid hormone syndrome
Ear, face and neck congenital anomalies
Congenital hypothyroidism due to peripheral resistance to thyroid hormone
Congenital iodine deficiency syndrome
Lysine methyltransferase 2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome

Frequently Asked Questions

What is the ICD-10 code for congenital hypothyroidism without goiter?

The ICD-10-CM code for congenital hypothyroidism without goiter is E03.1. The full clinical description is "Congenital hypothyroidism without goiter". E03.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E03.1 mean?

ICD-10-CM code E03.1 represents “Congenital hypothyroidism without goiter”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.

Is E03.1 a billable code?

Yes, E03.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is E03.1 in?

E03.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).

What codes cannot be used with E03.1?

E03.1 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); iodine-deficiency related hypothyroidism (E00-E02); postprocedural hypothyroidism (E89.0).

What SNOMED CT codes does E03.1 map to?

E03.1 maps to 44 SNOMED CT concepts: 204508009, 719098007, 26692000, 1281843005, 715734006, and 39 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for E03.1?

E03.1 is linked to 4 UMLS Concept Unique Identifiers: C0749420, C0010308, C0342151, C0342154. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does E03.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like congenital hypothyroidism without goiter affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E03.1?

E03.1 maps to the ICD-11 code: 5A00.01 (Permanent congenital hypothyroidism without goitre).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.