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56329008: Pituitary 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
93667018 Pituitary gland en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
93669015 Hypophysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
497589011 Pituitary structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
794829019 Pituitary structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
874071000172115 structure de l'hypophyse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
881891000172116 hypophyse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
913841000172115 glande pituitaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1018461000172117 hypophysis fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


52 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pituitary structure Is a Pituitary and/or pineal structures (body structure) true Inferred relationship Some
Pituitary structure Is a Hypothalamic structure false Inferred relationship Some
Pituitary structure partie de Entire diencephalon (body structure) false Additional relationship Some
Pituitary structure partie de Entire endocrine system false Additional relationship Some
Pituitary structure Is a Hypothalamus part false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Colloid cyst of pituitary gland (disorder) Finding site False Pituitary structure Inferred relationship Some 1
Invasive pituitary adenoma Finding site False Pituitary structure Inferred relationship Some 1
Colloid cyst of pituitary gland (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Functionless pituitary neoplasm (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Invasive pituitary adenoma Finding site False Pituitary structure Inferred relationship Some 1
Functioning pituitary neoplasm (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Pituicytoma Finding site True Pituitary structure Inferred relationship Some 1
Familial isolated pituitary adenoma Finding site True Pituitary structure Inferred relationship Some 1
Ectopic pituitary tissue Finding site False Pituitary structure Inferred relationship Some 2
Congenital absence of pituitary gland Finding site False Pituitary structure Inferred relationship Some 2
Accessory pituitary gland Finding site False Pituitary structure Inferred relationship Some 2
Congenital anomaly of pituitary gland Finding site False Pituitary structure Inferred relationship Some 2
Pharyngeal pituitary tissue Finding site False Pituitary structure Inferred relationship Some 4
Ectopic pituitary tissue Finding site True Pituitary structure Inferred relationship Some 1
A rare pituitary deficiency characterized by herniation of the subarachnoid space into the sella turcica, resulting in flattening of the pituitary gland and endocrine dysfunction. Most common endocrine abnormalities are hyperprolactinemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhea, obesity, and visual disturbances, among others. Finding site True Pituitary structure Inferred relationship Some 2
Choroideremia co-occurrent with hypopituitarism Finding site False Pituitary structure Inferred relationship Some
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. Finding site False Pituitary structure Inferred relationship Some
Hypopituitarism following procedure (disorder) Finding site True Pituitary structure Inferred relationship Some 2
Familial isolated pituitary adenoma Finding site False Pituitary structure Inferred relationship Some 2
Choroideremia co-occurrent with hypopituitarism Finding site False Pituitary structure Inferred relationship Some 1
Congenital hypopituitarism is characterized by multiple pituitary hormone deficiency, including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies. Congenital hypopituitarism is rare compared with the high incidence of hypopituitarism induced by pituitary adenomas, transsphenoidal surgery or radiotherapy. Finding site True Pituitary structure Inferred relationship Some 1
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. Finding site False Pituitary structure Inferred relationship Some 6
Hypopituitarism due to radiotherapy Finding site True Pituitary structure Inferred relationship Some 1
Pharyngeal pituitary tissue Finding site True Pituitary structure Inferred relationship Some 2
A rare genetic, syndromic retinal disorder characterized by the association of retinitis pigmentosa, hypopituitarism, nephronophthisis, and skeletal dysplasia. Finding site True Pituitary structure Inferred relationship Some 2
A rare midline cerebral malformation characterized by duplicated pituitary stalks and/or glands within duplicated sella. Patients may present various degrees of facial dysmorphism and endocrine abnormalities, including precocious puberty, hypogonadism, hypothyroidism and/or hyperprolactinemia, as well as associated congenital anomalies, such as clift lip/palate, bifid nasal bridge/tongue/uvula, hypothalamic enlargement with or without hamartoma, nasopharyngeal tumors, corpus callosum agenesis/hypoplasia, basilar artery duplication, and/or vertebral defects (in particular, duplication of the odontoid process). Finding site True Pituitary structure Inferred relationship Some 1
A rare, mixed, functioning pituitary adenoma characterized by the cosecretion of growth hormone and prolactin, which manifests with signs and symptoms of both acromegaly and hyperprolactinemia. Finding site True Pituitary structure Inferred relationship Some 1
Pituitary dermoid and epidermoid cysts is a rare, acquired pituitary hormone deficiency characterised by the presence of rare, benign tumour in the sellar region. Clinical presentation is either acute or insidious, and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances, and pituitary dysfunction. Finding site True Pituitary structure Inferred relationship Some 1
Pituitary dermoid and epidermoid cysts is a rare, acquired pituitary hormone deficiency characterised by the presence of rare, benign tumour in the sellar region. Clinical presentation is either acute or insidious, and is variable according to the cyst location, size and potential rupture. Most commonly patients present with headache, visual disturbances, and pituitary dysfunction. Finding site True Pituitary structure Inferred relationship Some 2
A rare, acquired pituitary hormone deficiency characterized by combination of headache, visual field defects that correlate with cyst size, and pituitary dysfunction. Most frequent hormonal manifestations are hypogonadism with amenorrhea/impotence or low libido and galactorrhea. Finding site True Pituitary structure Inferred relationship Some 1
Septo-optic dysplasia sequence Finding site True Pituitary structure Inferred relationship Some 1
Malignant pituitary blastoma (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Hypopituitarism caused by drug (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Epidermoid cyst of pituitary gland (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Transsphenoidal partial excision of neoplasm of pituitary gland (procedure) Procedure site - Direct (attribute) False Pituitary structure Inferred relationship Some 1
Transsphenoidal total excision of neoplasm of pituitary gland (procedure) Procedure site - Direct (attribute) True Pituitary structure Inferred relationship Some 1
Endoscopic endonasal transsphenoidal total excision of neoplasm of pituitary gland Procedure site - Direct (attribute) True Pituitary structure Inferred relationship Some 1
Endoscopic endonasal transsphenoidal partial excision of neoplasm of pituitary gland Procedure site - Direct (attribute) False Pituitary structure Inferred relationship Some 1
A benign tumor invasive into adjacent structures. Finding site True Pituitary structure Inferred relationship Some 1
Adenocarcinoma of pituitary gland Finding site True Pituitary structure Inferred relationship Some 1
Xanthogranulomatous hypophysitis (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Autoimmune hypopituitarism (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Hypopituitarism due to granulomatous disease Finding site True Pituitary structure Inferred relationship Some 1
Hypopituitarism due to metabolic disease (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Hypopituitarism due to vascular disorder Finding site True Pituitary structure Inferred relationship Some 1
Immunoglobulin G4 related hypophysitis (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Incision and exploration of pituitary gland Procedure site - Direct (attribute) True Pituitary structure Inferred relationship Some 2
Microprolactinoma Finding site True Pituitary structure Inferred relationship Some 2
Macroprolactinoma Finding site True Pituitary structure Inferred relationship Some 2
Prolactinoma Finding site True Pituitary structure Inferred relationship Some 2
Pituitary hypertrophy Finding site True Pituitary structure Inferred relationship Some 1
Pituitary degeneration Finding site True Pituitary structure Inferred relationship Some 1
Avascular necrosis of pituitary gland (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Isolated deficiency of pituitary hormone (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Metastatic carcinoma to pituitary (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Metastatic adenocarcinoma to pituitary gland (disorder) Finding site True Pituitary structure Inferred relationship Some 1
Primary adenocarcinoma of pituitary gland (disorder) Finding site True Pituitary structure Inferred relationship Some 1
A rare pituitary tumor characterized by the presence of a pituitary adenoma that has metastasized either within the central nervous system, or to distant sites. The vast majority of pituitary carcinomas are hormonally active, most frequently with ACTH or prolactin production. The most common clinical symptoms are diabetes insipidus, optic nerve dysfunction, anterior pituitary dysfunction, palsy of cranial nerves III, IV, or VI, and headaches, although patients may also be asymptomatic. The tumors behave aggressively, and prognosis is poor. Finding site True Pituitary structure Inferred relationship Some 1
Structure of transplanted pituitary gland (body structure) Is a True Pituitary structure Inferred relationship Some
Excision of neoplasm of pituitary (procedure) Procedure site - Direct (attribute) True Pituitary structure Inferred relationship Some 1
Magnetic resonance imaging of pituitary gland (procedure) Procedure site - Direct (attribute) True Pituitary structure Inferred relationship Some 1
Malignant neoplasm of pituitary and hypothalamus Finding site True Pituitary structure Inferred relationship Some 2
A rare, acquired pituitary hormone deficiency characterised by inflammation of the pituitary gland secondary to immunotherapy for cancer treatments (such as monoclonal antibodies against cytotoxic T lymphocytes antigen, programmed cell death protein-1, and programmed cell death ligand molecules). Major clinical features include headache, fatigue, adrenal insufficiency and hypothyroidism. Patients may also have nausea and vomiting associated to the headache as well as dizziness and hot flashes. Enlargement of the pituitary gland is present in the brain imaging. Finding site True Pituitary structure Inferred relationship Some 1
Inflammation of pituitary caused by drug (disorder) Finding site True Pituitary structure Inferred relationship Some 1

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Reference Sets

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

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

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