E03.1
BillableCongenital hypothyroidism without goiter
Congenital hypothyroidism without goiter
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Aplasia of thyroid (with myxedema)
- Congenital atrophy of thyroid
- Congenital hypothyroidism NOS
Also Known As / Clinical Terms
SNOMED CT
- Transient hypothyroidism2917005
- Central hypothyroidism26692000
- Hypertrophy of testis32121007
- Primary hypothyroidism57185003
- Congenital absence of thyroid gland92978002
- Congenital thyroid aplasia92978002
- Congenital hypothyroidism190268003
- Thyroid atrophy190309006
- Ear, face and neck congenital anomalies204223000
- Atresia of posterior nares204508009
- Atresia of posterior naris204508009
- Choanal atresia204508009
- Congenital atresia of choana204508009
- Congenital atresia of posterior nares204508009
- Neonatal jaundice with congenital hypothyroidism206457007
- Congenital goiter217710005
- Congenital goitre217710005
- Congenital hypothyroidism not due to iodine deficiency217710005
- Congenital iodine deficiency syndrome217710005
- Cretinism217710005
- Fetal iodine deficiency syndrome217710005
- Foetal iodine deficiency syndrome217710005
- Infantile hypothyroidism217710005
- Congenital hypothyroidism without goiter237515009
- Congenital hypothyroidism without goitre237515009
- Congenital thyroid hypoplasia237516005
- Congenital atrophy of thyroid237517001
- RTH (resistance to thyroid hormone) syndrome237559000
- Resistance to TH (thyroid hormone) syndrome237559000
- Resistance to thyroid hormone syndrome237559000
- Thyroid hormone resistance237559000
- Thyroid hormone resistance syndrome237559000
- Hypoplasia of thyroid367524008
- Developmental malformation of branchial arch402810002
- Infant hypothyroidism405629002
- Congenital absence of half of thyroid715734006
- Congenital hemiagenesis of thyroid715734006
- Thyroid hemiagenesis715734006
- Congenital hypothyroidism due to transplacental passage of maternal TSH (thyroid stimulating hormone)-binding inhibitory antibody717333002
- Congenital hypothyroidism due to transplacental passage of maternal thyroid stimulating hormone binding inhibitory antibody717333002
- Idiopathic congenital hypothyroidism717334008
- Familial thyroid dyshormonogenesis718183003
- Hypothyroidism due to mutation in transcription factor of pituitary development718194004
- Congenital hypothyroidism due to absence of thyroid gland718690009
- Brain lung thyroid syndrome719098007
- Choreoathetosis with congenital hypothyroidism and neonatal respiratory distress syndrome719098007
- Obesity, colitis, hypothyroidism, cardiac hypertrophy, developmental delay syndrome722051004
- Congenital central hypothyroidism722938007
- Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome724094005
- Congenital central hypothyroidism due to thyrotropin-releasing hormone receptor deficiency725462002
- Resistance to thyrotropin-releasing hormone syndrome725462002
- TRH (thyrotropin-releasing hormone) resistance syndrome725462002
- Genetic transient congenital hypothyroidism770631009
- IGSF1 (immunoglobulin superfamily member 1) deficiency syndrome771510006
- X-linked central congenital hypothyroidism with late-onset macroorchidism771510006
- X-linked central congenital hypothyroidism with late-onset testicular enlargement771510006
- Congenital hypothyroidism due to maternal intake of antithyroid drug783177006
- Transient congenital hypothyroidism due to dual oxidase 2 mutation1142106007
- Congenital hypothyroidism due to thyroid peroxidase mutation1179394003
- Congenital hypothyroidism due to thyroid deiodinase mutation1179396001
- Congenital hypothyroidism due to symporter mutation1179397005
- Congenital hypothyroidism due to thyroglobulin mutation1179399008
- Congenital hypothyroidism due to dual oxidase maturation factor 21179400001
- Congenital hypothyroidism due to peripheral resistance to thyroid hormone1179401002
- Congenital hypothyroidism due to congenital anomaly of thyroid gland1179404005
- Degeneration of thyroid1217042001
- Thyroid degeneration1217042001
- Congenital hypothyroidism due to thyroid stimulating hormone receptor mutation1230272009
- Hypothyroidism due to TSH receptor mutation1230272009
- Hypothyroidism due to TSHR (thyroid stimulating hormone receptor) mutation1230272009
- Resistance to thyroid hormone alpha1260240000
- Resistance to thyroid hormone due to mutation in TRa1260240000
- Resistance to thyroid hormone due to mutation in thyroid hormone receptor alpha1260240000
- Choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
- KMT2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
- Lysine methyltransferase 2D-related choanal atresia, athelia, hypothyroidism, delayed puberty, short stature syndrome1281843005
UMLS
- Agenesis, ThyroidC0749420
- Aplasia of thyroid (with myxedema)C0749420
- Congenital Thyroid AplasiaC0749420
- Congenital Thyroid Gland AplasiaC0749420
- Congenital absence of thyroid glandC0749420
- Congenital absence of thyroid gland (disorder)C0749420
- Congenital thyroid aplasiaC0749420
- THYROID AGENESISC0749420
- Thyroid AgenesisC0749420
- Thyroid agenesisC0749420
- agenesis thyroidC0749420
- thyroid agenesisC0749420
- CHTC0010308
- CONGEN HYPOTHYROIDISMC0010308
- Congenital HypothyroidismC0010308
- Congenital goiterC0010308
- Congenital goitreC0010308
- Congenital hypothyroidismC0010308
- Congenital hypothyroidism (disorder)C0010308
- Congenital hypothyroidism NOSC0010308
- Congenital hypothyroidism not due to iodine deficiencyC0010308
- CretinismC0010308
- Hypothyroidism congenitalC0010308
- Hypothyroidism, CongenitalC0010308
- Hypothyroidism, congenitalC0010308
- Infantile hypothyroidismC0010308
- Underactive thyroid gland from birthC0010308
- congenital hypothyroidismC0010308
- cretinismC0010308
- hypothyroidism congenitalC0010308
- infantile hypothyroidismC0010308
- Congenital Hypothyroidism without GoiterC0342151
- Congenital hypothyroidism without goiterC0342151
- Congenital hypothyroidism without goiter (disorder)C0342151
- Congenital hypothyroidism without goitreC0342151
- Congenital atrophy of thyroidC0342154
- Congenital atrophy of thyroid (disorder)C0342154
Frequently Asked Questions
What is ICD-10 code E03.1?
ICD-10-CM code E03.1 represents "Congenital hypothyroidism without goiter". It 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.
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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.