237705001: Hypophysitis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis
\Head finding (finding)\Disorder of head (disorder)\Inflammatory disorder of head\Hypophysitis
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis
\Central nervous system finding\Disorder of the central nervous system (disorder)\Inflammatory disease of the central nervous system\Hypophysitis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2004. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

356256014 Hypophysitis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

626473017 Hypophysitis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1879721000195111 ipofisite it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

5019741000241112 hypophysite fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

2414891000195118 Hypophysitis de Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hypophysitis	Is a	Disease of pituitary gland	false	Inferred relationship	Some
Hypophysitis	Finding site	Entire endocrine gonad (body structure)	false	Inferred relationship	Some
Hypophysitis	Finding site	Pituitary structure	false	Inferred relationship	Some	1
Hypophysitis	Is a	Inflammatory disorder	false	Inferred relationship	Some
Hypophysitis	Associated morphology	inflammation	false	Inferred relationship	Some	1
Hypophysitis	Is a	Encephalitis	false	Inferred relationship	Some
Hypophysitis	Is a	Disorder of pituitary gland	true	Inferred relationship	Some
Hypophysitis	Is a	Limbic encephalitis	false	Inferred relationship	Some
Hypophysitis	Associated morphology	inflammation	false	Inferred relationship	Some	1
Hypophysitis	Finding site	Pituitary structure	true	Inferred relationship	Some	1
Hypophysitis	Associated morphology	Inflammatory morphology (morphologic abnormality)	true	Inferred relationship	Some	1
Hypophysitis	Is a	Inflammation of specific body organs	true	Inferred relationship	Some
Hypophysitis	Is a	Inflammatory disorder of head	true	Inferred relationship	Some
Hypophysitis	Is a	Inflammatory disease of the central nervous system	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Autoimmune hypophysitis	Is a	True	Hypophysitis	Inferred relationship	Some
Granulomatous giant-cell hypophysitis	Is a	True	Hypophysitis	Inferred relationship	Some
Lymphocytic hypopituitarism	Is a	True	Hypophysitis	Inferred relationship	Some
A type of primary hypophysitis characterised by an inflammation of the entire pituitary gland. Common clinical presentation is diabetes insipidus with polyuria and polydipsia and partial or panhypopituitarism. Other symptoms may include headaches, nausea/vomiting, visual disturbances and fatigue.	Is a	True	Hypophysitis	Inferred relationship	Some
A type of primary hypophysitis characterized by an inflammation of the posterior pituitary and the stalk. The major clinical manifestation is diabetes insipidus with polyuria and polydipsia. Less frequent symptoms are headaches, adrenal insufficiency, hyperprolactinemia and hypogonadism.	Is a	True	Hypophysitis	Inferred relationship	Some
A rare, acquired pituitary hormone deficiency, a type of primary hypophysitis characterized by an inflammation of anterior pituitary. Clinical presentation is variable and includes headaches, visual disturbances, symptoms of adrenal insufficiency, hyperprolactinemia, hypothyroidism and hypogonadism. It most commonly affects young women during pregnancy or postpartum period.	Is a	True	Hypophysitis	Inferred relationship	Some
Xanthogranulomatous hypophysitis (disorder)	Is a	True	Hypophysitis	Inferred relationship	Some
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.	Is a	False	Hypophysitis	Inferred relationship	Some
Inflammation of pituitary caused by drug (disorder)	Is a	True	Hypophysitis	Inferred relationship	Some

This concept is not in any reference sets