FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.3  |  FHIR Version n/a  User: [n/a]

69748006: Thyroid structure (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
115856014 Thyroid gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
115859019 Thyroid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
501376015 Thyroid structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
809727012 Thyroid structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3920511000005112 struktur af thyroidea da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


69 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Thyroid structure Is a Thyroid and/or parathyroid structures (body structure) true Inferred relationship Some
Thyroid structure Is a Endocrine gland of neck false Inferred relationship Some
Thyroid structure Is a Neck structure false Inferred relationship Some
Thyroid structure del af Entire endocrine system false Additional relationship Some
Thyroid structure del af Entire neck false Additional relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Inherited disorder of thyroid metabolism Finding site True Thyroid structure Inferred relationship Some 1
X-linked reduction of thyroxine-binding globulin Finding site True Thyroid structure Inferred relationship Some 1
Thyroglobulin proteolysis defect Finding site True Thyroid structure Inferred relationship Some 1
Thyroid hormone responsiveness defect Finding site True Thyroid structure Inferred relationship Some 1
Iodide oxidation defect Finding site True Thyroid structure Inferred relationship Some 1
X-linked excess of thyroxine-binding globulin Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to defect in thyroid hormone synthesis Finding site True Thyroid structure Inferred relationship Some 1
Thyroxine transport defect Finding site True Thyroid structure Inferred relationship Some 1
Multiple endocrine neoplasia, type 2b Finding site False Thyroid structure Inferred relationship Some 2
Autosomal dominant excess of transthyretin Finding site True Thyroid structure Inferred relationship Some 1
X-linked variant form of thyroxine-binding globulin (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Thyroxine plasma membrane transport defect Finding site True Thyroid structure Inferred relationship Some 1
Iodide peroxidase defect Finding site True Thyroid structure Inferred relationship Some 1
Refetoff syndrome Finding site True Thyroid structure Inferred relationship Some 1
Thyroid hormone resistance syndrome Finding site True Thyroid structure Inferred relationship Some 1
Generalized thyroid hormone resistance Finding site True Thyroid structure Inferred relationship Some 1
Pituitary thyroid hormone resistance Finding site True Thyroid structure Inferred relationship Some 1
Thyrotoxicosis due to pituitary thyroid hormone resistance Finding site True Thyroid structure Inferred relationship Some 1
A rare hyperthyroidism characterized by mild to severe hyperthyroidism, presence of goiter, absence of features of autoimmunity, frequent relapses while on treatment and a positive family history. Finding site True Thyroid structure Inferred relationship Some 1
Familial thyroid dyshormonogenesis is a type of primary congenital hypothyroidism, a permanent thyroid hormone deficiency that is present from birth, which results from inborn errors of thyroid hormone synthesis. Finding site True Thyroid structure Inferred relationship Some 1
Peripheral resistance to thyroid hormone (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to mutations in transcription factors involved in pituitary development or function is a type of central congenital hypothyroidism, a permanent thyroid deficiency that is present from birth, characterized by low levels of thyroid hormones caused by disorders in the development or function of the pituitary. Finding site True Thyroid structure Inferred relationship Some 1
Thyroid cyst fluid specimen (specimen) Specimen source topography (attribute) True Thyroid structure Inferred relationship Some 2
An extremely rare inherited tumor syndrome within the familial nonmedullary thyroid cancer group. Finding site False Thyroid structure Inferred relationship Some 1
Removal of thyroid nodule Procedure site - Direct (attribute) False Thyroid structure Inferred relationship Some 2
Mixed follicular and papillary thyroid carcinoma Finding site True Thyroid structure Inferred relationship Some 2
Open biopsy of thyroid (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Hyperthyroidism in pregnancy (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Percutaneous needle biopsy of thyroid using computed tomography guidance (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 2
Percutaneous needle biopsy of thyroid using computed tomography guidance (procedure) Procedure site - Direct (attribute) False Thyroid structure Inferred relationship Some 3
Hypothyroidism following external radiotherapy (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by radiation Finding site True Thyroid structure Inferred relationship Some 2
Hypothyroidism following radioiodine therapy Finding site True Thyroid structure Inferred relationship Some 2
Radionuclide imaging of thyroid using iodine-123 (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using iodine-131 (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Static radionuclide imaging of thyroid Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using technetium (99m-Tc) sodium pertechnetate Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using iodine radioisotope Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using iodine-125 (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using technetium (99m-Tc) succimer (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using technetium radioisotope (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using technetium-99 (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using technetium-99m (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid using thallium-201 Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 1
Radionuclide imaging of thyroid with administration of thyrotropin releasing hormone (procedure) Procedure site - Direct (attribute) True Thyroid structure Inferred relationship Some 2
Radionuclide imaging of thyroid with administration of thyrotropin releasing hormone (procedure) Procedure site - Direct (attribute) False Thyroid structure Inferred relationship Some 1
Short stature-delayed bone age due to thyroid hormone metabolism deficiency is a rare, genetic congenital hypothyroidism disorder characterized by mild global developmental delay in childhood, short stature, delayed bone age, and abnormal thyroid and selenium levels in serum (high total and free T4 concentrations, low T3, high reverse T3, normal to high TSH, decreased selenium). Intellectual disability, primary infertility, hypotonia, muscle weakness, and impaired hearing have also been reported. Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to fibrous invasive thyroiditis Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by radiation Finding site False Thyroid structure Inferred relationship Some 3
Autoimmune hypothyroidism Finding site True Thyroid structure Inferred relationship Some 1
Iodine hypothyroidism Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to Hashimoto's thyroiditis Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to TSH receptor blocking antibody Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism resulting from para-aminosalicylic acid Finding site True Thyroid structure Inferred relationship Some 1
kompenseret hypotyroidisme Finding site False Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by resorcinol (disorder) Finding site True Thyroid structure Inferred relationship Some 1
kompenseret eutyroidisme Finding site False Thyroid structure Inferred relationship Some 1
Transient decreased production of T>4< Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to sarcoidosis Finding site True Thyroid structure Inferred relationship Some 1
Transient decreased production of T>3< Finding site True Thyroid structure Inferred relationship Some 1
Iatrogenic hypothyroidism Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to infiltrative disease Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism following radioiodine therapy Finding site False Thyroid structure Inferred relationship Some 3
Hypothyroidism due to thyroiditis (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Euthyroid with thyroid antibodies Finding site True Thyroid structure Inferred relationship Some 1
Postablative hypothyroidism Finding site True Thyroid structure Inferred relationship Some 2
Hypothyroidism caused by food stuff (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism following external radiotherapy (disorder) Finding site False Thyroid structure Inferred relationship Some 3
Hypothyroidism due to scleroderma Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism resulting from phenylbutazone Finding site True Thyroid structure Inferred relationship Some 1
Acquired central hypothyroidism (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Subclinical iodine deficiency hypothyroidism (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Acquired hypothyroidism (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by iodide excess Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by drug (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Post-infectious hypothyroidism Finding site True Thyroid structure Inferred relationship Some 1
Idiopathic atrophic hypothyroidism Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to amyloidosis Finding site True Thyroid structure Inferred relationship Some 1
Postoperative hypothyroidism (disorder) Finding site True Thyroid structure Inferred relationship Some 1
Hypothyroidism due to cystinosis Finding site True Thyroid structure Inferred relationship Some 1
Genetic transient congenital hypothyroidism is a rare, thyroid disease characterized by a gene mutation induced, temporary deficiency of thyroid hormones at birth, which later reverts to normal with or without replacement therapy in the first few months or years of life. Finding site True Thyroid structure Inferred relationship Some 1
A rare acquired neurological disease with characteristics of encephalopathy associated with elevated antithyroid antibodies, in the absence of other causes. Clinical presentation varies from minor cognitive impairment to status epilepticus and coma, and frequently includes seizures, confusion, speech disorder, memory impairment, ataxia and psychiatric manifestations. Finding site True Thyroid structure Inferred relationship Some 2
Tuberculosis of thyroid gland (disorder) Finding site True Thyroid structure Inferred relationship Some 1
A rare genetic endocrine disease with characteristics of central hypothyroidism, testis enlargement in adolescence resulting in adult macroorchidism, delayed pubertal testosterone rise with a subsequent delayed pubertal growth spurt, small thyroid gland, and variable prolactin and growth hormone deficiency. Caused by mutation in the IGSF1 gene on chromosome Xq26. Finding site True Thyroid structure Inferred relationship Some 2
Obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome is characterized by precocious obesity, congenital hypothyroidism, neonatal colitis, cardiac hypertrophy, craniosynostosis and developmental delay. It has been described in two brothers, one of whom died within the first month of life. The parents of the two children were nonconsanguineous and in good health, however, the pregnancies were complicated by a maternal HELLP syndrome (Haemolysis, Elevated Liver enzymes and Low Platelets). The mode of inheritance has not yet been clearly established. Finding site True Thyroid structure Inferred relationship Some 4
Multinodular goiter - cystic kidney - polydactyly syndrome is a very rare syndrome characterized by the association of multinodular goiter, cystic renal disease and digital anomalies. Finding site False Thyroid structure Inferred relationship Some 2
Primary differentiated carcinoma of thyroid gland (disorder) Finding site True Thyroid structure Inferred relationship Some 1
A rare endocrine disease with characteristics of the appearance of transient hypothyroidism usually in preterm newborns following long or short-term topical iodine exposure. Parenteral exposure from iodinated contrast agents may similarly alter thyroid function in term neonates. Finding site True Thyroid structure Inferred relationship Some 1
Removal of thyroid adenoma (procedure) Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Excision of adenoma of thyroid Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Excision of cyst of thyroid Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Operation on lesion of thyroid gland Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Removal of thyroid nodule Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Excision of lesion of thyroid Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Incision of lesion of thyroid gland Procedure site - Indirect (attribute) True Thyroid structure Inferred relationship Some 1
Hypothyroidism caused by amiodarone Finding site True Thyroid structure Inferred relationship Some 1
A rare congenital hypothyroidism disorder with characteristics of transient primary fetal or neonatal hypothyroidism resulting from transplacental transfer of antithyroid drugs due to maternal intake. Patients may present fetal or neonatal goitre, hoarse cry, reduced tendon reflexes, feeding difficulty, constipation, prolonged jaundice and/or respiratory distress. Elevated levels of T4 and thyroid stimulating hormone usually normalise without treatment within 3 weeks of birth. Finding site True Thyroid structure Inferred relationship Some 1
Thyroid infection Finding site True Thyroid structure Inferred relationship Some 1
A rare hereditary nonmedullary thyroid carcinoma characterised by the presence of differentiated thyroid cancer of follicular cell origin in two or more first-degree relatives, in the absence of other familial tumour syndromes or radiation exposure. Frequent capsular invasion is observed. Biopsy reveals multicentric tumours with multiple adenomatous nodules with or without oxyphilia and follicular or papillary carcinoma histology. Finding site True Thyroid structure Inferred relationship Some 1
Congenital iodine deficiency syndrome Finding site True Thyroid structure Inferred relationship Some 1
Congenital hypothyroidism without goitre Finding site True Thyroid structure Inferred relationship Some 1

Start Previous Page 14 of 16 Next End


Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

Back to Start