E07.89
BillableOther specified disorders of thyroid
Other specified disorders of thyroid
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Abnormality of thyroid-binding globulin
- Hemorrhage of thyroid
- Infarction of thyroid
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(1)
Also Known As / Clinical Terms(202)
SNOMED CT
- X-linked absence of thyroxine-binding globulin2241003
- Haemorrhage of thyroid3002002
- Hemorrhage of thyroid3002002
- Thyroid haemorrhage3002002
- Thyroid hemorrhage3002002
- Infarction of thyroid11859008
- Thyroid infarction11859008
- Hurthle cell metaplasia of thyroid gland19608008
- Ascher syndrome28599006
- Ascher's syndrome28599006
- Blepharochalasis and double lip28599006
- X-linked reduction of thyroxine-binding globulin41300001
- Thyroglobulin proteolysis defect43449002
- Congenital unresponsiveness to thyrotropin50375007
- Hypothyroidism due to thyroid insensitivity to TSH (thyroid stimulating hormone)50375007
- Thyroid hormone responsiveness defect50375007
- Thyroid hormone unresponsiveness50375007
- Unresponsiveness of thyroid gland to thyrotropin50375007
- X-linked excess of thyroxine-binding globulin55296004
- Thyroxine transport defect56112001
- Autosomal dominant excess of thyroxine-binding prealbumin66185005
- Autosomal dominant excess of transthyretin66185005
- Decrease thyroid hormone production associated with illness70953003
- Transient decreased production of thyroid hormone70953003
- X-linked variant form of thyroxine-binding globulin73068003
- Thyroxine plasma membrane transport defect79488001
- Intrathyroidal calcification AND goiter syndrome80304004
- Intrathyroidal calcification AND goitre syndrome80304004
- Complex thyroid endocrine disorder123766008
- Thyroid-binding globulin abnormality190308003
- Thyroid hormone binding abnormality237543000
- Thyroid-binding globulin deficiency237544006
- Drug interference with thyroid-binding globulin237545007
- Thyroid-binding globulin high237546008
- Thyroid pre-albumin binding abnormality237548009
- Dysprealbuminaemic euthyroidal hyperthyroxinaemia237549001
- Dysprealbuminemic euthyroidal hyperthyroxinemia237549001
- Euthyroid hypothyroxinaemia237550001
- Euthyroid hypothyroxinemia237550001
- Euthyroid hyperthyroxinaemia237551002
- Euthyroid hyperthyroxinemia237551002
- RTH (resistance to thyroid hormone) syndrome237559000
- Resistance to TH (thyroid hormone) syndrome237559000
- Resistance to thyroid hormone syndrome237559000
- Thyroid hormone resistance237559000
- Thyroid hormone resistance syndrome237559000
- General resistance to thyrotropin237560005
- Generalised thyroid hormone resistance237560005
- Generalized thyroid hormone resistance237560005
- Refetoff syndrome237560005
- Thyroid gland haematoma262773008
- Thyroid gland hematoma262773008
- Neck swelling301777002
- Finding of appearance of thyroid gland302066004
- Observation of appearance of thyroid gland302066004
- Finding of size of thyroid gland302067008
- Observation of size of thyroid gland302067008
- Small thyroid gland302068003
- Raised TSH (thyroid stimulating hormone) level309080005
- Raised thyroid stimulating hormone level309080005
- Thyroid stimulating hormone level above reference range309080005
- Pituitary thyroid hormone resistance360348000
- Eyelid malposition404625000
- Haematoma of neck447220009
- Hematoma of neck447220009
- Congenital double lip699762000
- Double lip699762000
- Peripheral resistance to thyroid hormone718193005
- Congenital malposition of eyelid726406009
- Cutler Bass Romshe syndrome733096007
- Thyrocerebrorenal syndrome733096007
- Bilateral swelling of lobes of thyroid833288009
- Swelling of bilateral lobes of thyroid gland833288009
- Swelling of left and right lobes of thyroid833288009
- Follicular lesion of thyroid1148693003
- Haemorrhagic infarction1162785009
- Hemorrhagic infarction1162785009
- Congenital hypothyroidism due to peripheral resistance to thyroid hormone1179401002
- Degeneration of thyroid1217042001
- Thyroid degeneration1217042001
- Gangrene of thyroid1217064005
- Thyroid gangrene1217064005
- Resistance to thyroid hormone beta1260241001
- Resistance to thyroid hormone due to mutation in TRb1260241001
- Resistance to thyroid hormone due to mutation in thyroid hormone receptor beta1260241001
- RTSH - resistance to thyroid stimulating hormone1366539009
- Resistance to TSH (thyroid stimulating hormone) syndrome1366539009
- Resistance to thyroid stimulating hormone syndrome1366539009
- Resistance to thyrotrophin syndrome1366539009
- Resistance to thyrotropin syndrome1366539009
- Haemorrhagic infarction of thyroid228156681000119109
- Hemorrhagic infarction of thyroid228156681000119109
UMLS
- Abnormality of thyroid-binding globulinC0342181
- Thyroid-binding globulin abnormalityC0342181
- Thyroid-binding globulin abnormality (disorder)C0342181
- Haemorrhage of thyroidC0271820
- Hemorrhage of thyroidC0271820
- Hemorrhage of thyroid (disorder)C0271820
- Thyroid bleedingC0271820
- Thyroid haemorrhageC0271820
- Thyroid hemorrhageC0271820
- Infarction of thyroidC0271821
- Infarction of thyroid (disorder)C0271821
- Thyroid infarctionC0271821
- Other specified disorders of thyroidC0154167
Clinical Terms
- Thyroid-binding globulin abnormality (disorder)
- Thyroid hormone responsiveness defect
- Resistance to thyroid hormone due to mutation in TRb
- Hemorrhage of thyroid
- Thyroid haemorrhage
- Infarction of thyroid (disorder)
- Observation of appearance of thyroid gland
- Resistance to thyroid hormone beta
- Hemorrhage of thyroid (disorder)
- Thyroglobulin proteolysis defect
- Thyroid bleeding
- Dysprealbuminaemic euthyroidal hyperthyroxinaemia
- Resistance to thyrotrophin syndrome
- Finding of appearance of thyroid gland
- Thyroxine transport defect
- Transient decreased production of thyroid hormone
- Resistance to thyroid hormone due to mutation in thyroid hormone receptor beta
- Haemorrhagic infarction of thyroid
- Hemorrhagic infarction of thyroid
- Follicular lesion of thyroid
- Pituitary thyroid hormone resistance
- Gangrene of thyroid
- Intrathyroidal calcification AND goitre syndrome
- Thyroid-binding globulin abnormality
- Thyroid hormone resistance syndrome
- Neck swelling
- Autosomal dominant excess of thyroxine-binding prealbumin
- Intrathyroidal calcification AND goiter syndrome
- Blepharochalasis and double lip
- Thyroid gland hematoma
- Observation of size of thyroid gland
- Ascher's syndrome
- Cutler Bass Romshe syndrome
- X-linked variant form of thyroxine-binding globulin
- Euthyroid hypothyroxinaemia
- Thyroid gland haematoma
- Thyroid-binding globulin high
- Abnormality of thyroid-binding globulin
- Decrease thyroid hormone production associated with illness
- Hemorrhagic infarction
- Unresponsiveness of thyroid gland to thyrotropin
- Complex thyroid endocrine disorder
- Raised thyroid stimulating hormone level
- Thyroid hormone unresponsiveness
- X-linked reduction of thyroxine-binding globulin
- X-linked excess of thyroxine-binding globulin
- Thyroid stimulating hormone level above reference range
- Drug interference with thyroid-binding globulin
- Raised TSH (thyroid stimulating hormone) level
- Euthyroid hyperthyroxinaemia
- Thyroid infarction
- Resistance to TH (thyroid hormone) syndrome
- Eyelid malposition
- Small thyroid gland
- Degeneration of thyroid
- Thyroid degeneration
- Euthyroid hyperthyroxinemia
- RTSH - resistance to thyroid stimulating hormone
- Bilateral swelling of lobes of thyroid
- Resistance to TSH (thyroid stimulating hormone) syndrome
- Congenital unresponsiveness to thyrotropin
- Generalized thyroid hormone resistance
- Infarction of thyroid
- Haematoma of neck
- Hurthle cell metaplasia of thyroid gland
- Euthyroid hypothyroxinemia
- X-linked absence of thyroxine-binding globulin
- Finding of size of thyroid gland
- Resistance to thyrotropin syndrome
- Swelling of left and right lobes of thyroid
- Thyrocerebrorenal syndrome
- Dysprealbuminemic euthyroidal hyperthyroxinemia
- Ascher syndrome
- Hypothyroidism due to thyroid insensitivity to TSH (thyroid stimulating hormone)
- Congenital double lip
- Congenital malposition of eyelid
- Thyroid hormone binding abnormality
- Thyroid hemorrhage
- General resistance to thyrotropin
- Refetoff syndrome
- RTH (resistance to thyroid hormone) syndrome
- Peripheral resistance to thyroid hormone
- Thyroid-binding globulin deficiency
- Thyroid gangrene
- Haemorrhage of thyroid
- Haemorrhagic infarction
- Autosomal dominant excess of transthyretin
- Thyroid hormone resistance
- Double lip
- Thyroxine plasma membrane transport defect
- Swelling of bilateral lobes of thyroid gland
- Thyroid pre-albumin binding abnormality
- Resistance to thyroid stimulating hormone syndrome
- Generalised thyroid hormone resistance
- Resistance to thyroid hormone syndrome
- Hematoma of neck
- Congenital hypothyroidism due to peripheral resistance to thyroid hormone
Frequently Asked Questions
What is the ICD-10 code for other specified disorders of thyroid?
The ICD-10-CM code for other specified disorders of thyroid is E07.89. The full clinical description is "Other specified disorders of thyroid". E07.89 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E07.89 mean?
ICD-10-CM code E07.89 represents “Other specified disorders of thyroid”. 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 E07.89 a billable code?
Yes, E07.89 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E07.89 in?
E07.89 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E07.89?
E07.89 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74).
What SNOMED CT codes does E07.89 map to?
E07.89 maps to 49 SNOMED CT concepts: 28599006, 66185005, 833288009, 123766008, 699762000, and 44 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E07.89?
E07.89 is linked to 4 UMLS Concept Unique Identifiers: C0342181, C0271820, C0271821, C0154167. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E07.89 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other specified disorders of thyroid 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 E07.89?
There is no direct ICD-11 mapping available for E07.89 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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.