783158009: Infundibulo neurohypophysitis (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Head finding (finding)\Disorder of head (disorder)\Inflammatory disorder of head\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Central nervous system finding\Disorder of the central nervous system (disorder)\Inflammatory disease of the central nervous system\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of body system\Inflammation of specific body systems\Inflammatory disease of the central nervous system\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of body system\Disorder of endocrine system\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Inflammatory disease of the central nervous system\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammatory disorder of head\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body systems\Inflammatory disease of the central nervous system\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Inflammatory disorder\Inflammation of specific body structures or tissue\Inflammation of specific body organs\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of head (disorder)\Inflammatory disorder of head\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.
• \Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Disorder of pituitary gland\Hypophysitis\A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3757878019	A rare acquired pituitary hormone deficiency, a type of primary hypophysitis characterised 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, hyperprolactinaemia and hypogonadism.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3757880013	A rare acquired pituitary hormone deficiency, 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.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3757879010	Infundibulo neurohypophysitis (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3757881012	Infundibulo neurohypophysitis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

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