AutoICD API

E07.1

Billable

Dyshormogenetic goiter

Dyshormogenetic goiter

Status

Billable / Specific

Block

E00-E07

Parent Code

E07

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Dyshormonogenetic goiter
  • Familial dyshormogenetic goiter
  • Familial dyshormonogenetic goiter
  • Pendred's syndrome

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Related Codes(3)
E07.0

Hypersecretion of calcitonin

BillableE07.8

Other specified disorders of thyroid

E07.9

Disorder of thyroid, unspecified

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

5A00.00Permanent congenital hypothyroidism with diffuse goitreequivalentPrimary
Also Known As / Clinical Terms(123)

SNOMED CT

UMLS

Clinical Terms

  • Hypothyroidism due to defect in thyroid hormone synthesis
  • Dyshormonogenic goiter
  • THYROID HORMONOGENESIS, GENETIC DEFECT IN, 2B
  • Hypothyroidism due to iodide trapping defect
  • GDTH IIB
  • TDH2B
  • pendreds syndrome
  • Genetic defect in thyroid hormonogenesis V
  • Congenital thyroid hormone coupling defect
  • HYPOTHYROIDISM, CONGENITAL, DUE TO DYSHORMONOGENESIS, 2B
  • Autosomal recessive sensorineural hearing impairment, enlarged vestibular aqueduct, and goiter
  • Hypothyroidism due to iodotyrosine deiodinase defect
  • pendred syndrome
  • Genetic defect in thyroid hormonogenesis IV
  • Iodotyrosine deiodinase deficiency
  • Hypothyroidism due to thyroglobulin biosynthetic defect
  • DEAFNESS WITH GOITER
  • THYROID DYSHORMONOGENESIS 2B
  • Hypothyroidism with sensorineural deafness
  • Pendred's syndrome (disorder)
  • Autosomal Recessive Sensorineural Hearing Impairment and Goiter
  • Familial dyshormogenetic goiter
  • GOITER-DEAFNESS SYNDROME
  • Hypothyroidism due to iodide organification defect
  • Familial dyshormonogenetic goiter
  • Hypothyroidism due to defective thyroid hormonogenesis
  • Familial dyshormonogenetic goiter (disorder)
  • PDS
  • Deiodinase deficiency
  • Genetic defect in thyroid hormonogenesis III
  • Familial dyshormonogenetic goitre
  • Iodotyrosyl coupling defect
  • Thyroglobulin synthesis defect
  • Goitre-deafness syndrome
  • Thyroid hormone organification defect II B
  • Pendred's Syndrome
  • Dyshormonogenic goitre
  • Iodotyrosine deiodination defect
  • Genetic defect in thyroid hormonogenesis II B
  • Dyshormonogenic goiter (disorder)
  • Dyshormonogenetic goiter AND iodide leak
  • Thyroid hormone coupling defect
  • Hypothyroidism due to thyroglobulin synthesis defect
  • Hypothyroidism due to deiodase defect
  • Dyshormonogenetic goitre AND iodide leak
  • Dyshormonogenetic goiter
  • Primary hypothyroidism
  • GDTH III - genetic defect in thyroid hormonogenesis III
  • Hypothyroidism due to coupling defect
  • Iodotyrosine dehalogenase deficiency
Frequently Asked Questions
What is the ICD-10 code for dyshormogenetic goiter?

The ICD-10-CM code for dyshormogenetic goiter is E07.1. The full clinical description is "Dyshormogenetic goiter". E07.1 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code E07.1 mean?

ICD-10-CM code E07.1 represents “Dyshormogenetic 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 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.

How does E07.1 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like dyshormogenetic 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 E07.1?

E07.1 maps to the ICD-11 code: 5A00.00 (Permanent congenital hypothyroidism with diffuse 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.