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715668008: Pituitary deficiency due to empty sella turcica syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303354017 Pituitary deficiency due to empty sella turcica syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303356015 Pituitary deficiency due to empty sella turcica syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303357012 Hypopituitarism due to empty sella turcica syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5401027016 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401028014 A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3303354017 Pituitary deficiency due to empty sella turcica syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303354017 Pituitary deficiency due to empty sella turcica syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303356015 Pituitary deficiency due to empty sella turcica syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303356015 Pituitary deficiency due to empty sella turcica syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303357012 Hypopituitarism due to empty sella turcica syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3303357012 Hypopituitarism due to empty sella turcica syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303358019 Pituitary deficiency due to a disorder that involves the sella turcica, a bony structure at the base of the brain that surrounds and protects the pituitary gland. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401027016 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401028014 A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3386641001000112 Hypophysenfunktionsstörung durch Empty-Sella-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
883871000172118 hypopituitarisme associé au syndrome de la selle turcique vide fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932591000172110 déficit hypophysaire associé au syndrome de la selle turcique vide fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
883871000172118 hypopituitarisme associé au syndrome de la selle turcique vide fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932591000172110 déficit hypophysaire associé au syndrome de la selle turcique vide fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386641001000112 Hypophysenfunktionsstörung durch Empty-Sella-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. Due to Empty sella syndrome true Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. Is a Hypopituitarism true Inferred relationship Existential restriction modifier (core metadata concept)
A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. Finding site Pituitary structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare pituitary deficiency characterised 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 hyperprolactinaemia and growth hormone deficit. Clinical symptoms are highly variable and include headaches, irregular menstruation, galactorrhoea, obesity, and visual disturbances, among others. Is a Central nervous system complication true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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