E07.1
BillableDyshormogenetic goiter
Dyshormogenetic goiter
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Dyshormonogenetic goiter
- Familial dyshormogenetic goiter
- Familial dyshormonogenetic goiter
- Pendred's syndrome
Also Known As / Clinical Terms
SNOMED CT
- Dyshormonogenetic goiter AND iodide leak8868001
- Dyshormonogenetic goitre AND iodide leak8868001
- Deiodinase deficiency17885001
- Genetic defect in thyroid hormonogenesis IV17885001
- Hypothyroidism due to deiodase defect17885001
- Hypothyroidism due to iodotyrosine deiodinase defect17885001
- Iodotyrosine dehalogenase deficiency17885001
- Iodotyrosine deiodinase deficiency17885001
- Iodotyrosine deiodination defect17885001
- Congenital thyroid hormone coupling defect23536000
- GDTH III - genetic defect in thyroid hormonogenesis III23536000
- Genetic defect in thyroid hormonogenesis III23536000
- Hypothyroidism due to coupling defect23536000
- Iodotyrosyl coupling defect23536000
- Thyroid hormone coupling defect23536000
- Hypothyroidism due to defect in thyroid hormone synthesis56041007
- Hypothyroidism due to defective thyroid hormonogenesis56041007
- Primary hypothyroidism57185003
- Genetic defect in thyroid hormonogenesis V63127008
- Hypothyroidism due to thyroglobulin biosynthetic defect63127008
- Hypothyroidism due to thyroglobulin synthesis defect63127008
- Thyroglobulin synthesis defect63127008
- GDTH IIB70348004
- Genetic defect in thyroid hormonogenesis II B70348004
- Goiter-deafness syndrome70348004
- Goitre-deafness syndrome70348004
- Hypothyroidism with sensorineural deafness70348004
- Pendred syndrome70348004
- Pendred's syndrome70348004
- Thyroid hormone organification defect II B70348004
- Dyshormonogenic goiter190304001
- Dyshormonogenic goitre190304001
- Familial dyshormonogenetic goiter237554005
- Familial dyshormonogenetic goitre237554005
- Hypothyroidism due to iodide trapping defect237555006
- Hypothyroidism due to iodide organification defect237556007
UMLS
- TDH2BC0271829
- Autosomal Recessive Sensorineural Hearing Impairment and GoiterC0271829
- Autosomal recessive sensorineural hearing impairment, enlarged vestibular aqueduct, and goiterC0271829
- DEAFNESS WITH GOITERC0271829
- Deafness with goiterC0271829
- GDTH IIBC0271829
- GOITER-DEAFNESS SYNDROMEC0271829
- Genetic defect in thyroid hormonogenesis II BC0271829
- Goiter-deafness syndromeC0271829
- Goitre-deafness syndromeC0271829
- HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2BC0271829
- Hypothyroidism with sensorineural deafnessC0271829
- Hypothyroidism, Congenital, Due To Dyshormonogenesis, 2BC0271829
- PDSC0271829
- PENDRED SYNDROMEC0271829
- Pendred SyndromeC0271829
- Pendred syndromeC0271829
- Pendred's SyndromeC0271829
- Pendred's syndromeC0271829
- Pendred's syndrome (disorder)C0271829
- THYROID DYSHORMONOGENESIS 2BC0271829
- THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2BC0271829
- Thyroid Dyshormonogenesis 2BC0271829
- Thyroid Hormonogenesis, Genetic Defect In, 2BC0271829
- Thyroid hormone organification defect II BC0271829
- pendred syndromeC0271829
- pendred's syndromeC0271829
- pendreds syndromeC0271829
- Dyshormogenetic goiterC0152077
- Dyshormonogenetic goiterC0152077
- Dyshormonogenic goiterC0152077
- Dyshormonogenic goiter (disorder)C0152077
- Dyshormonogenic goitreC0152077
- Familial dyshormogenetic goiterC2873879
- Familial dyshormonogenetic goiterC0342191
- Familial dyshormonogenetic goiter (disorder)C0342191
- Familial dyshormonogenetic goitreC0342191
Frequently Asked Questions
What is ICD-10 code E07.1?
ICD-10-CM code E07.1 represents "Dyshormogenetic goiter". It is a billable/specific code that can be used on a claim.
Is E07.1 a billable code?
Yes, E07.1 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E07.1 in?
E07.1 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E07.1?
E07.1 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); transitory congenital goiter with normal function (P72.0).
What SNOMED CT codes does E07.1 map to?
E07.1 maps to 11 SNOMED CT concepts: 23536000, 17885001, 8868001, 190304001, 237554005, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E07.1?
E07.1 is linked to 4 UMLS Concept Unique Identifiers: C0271829, C0152077, C2873879, C0342191. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.