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1356806004: Entire sella turcica (body structure)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Jan 2025. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5429475014 Entire sella turcica (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5429476010 Entire sella turcica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5429475014 Entire sella turcica (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5429476010 Entire sella turcica en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Entire sella turcica (body structure) Is a Structure of sella turcica true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Short stature-pituitary and cerebellar defects-small sella turcica syndrome is characterized by short stature, anterior pituitary hormone deficiency, small sella turcica, and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of a large French kindred. Ectopia of the posterior hypophysis was observed in some patients. The syndrome is transmitted as a dominantly inherited trait and is caused by a germline mutation within the LIM-homeobox transcription factor LHX4 gene (1q25). Finding site False Entire sella turcica (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1
Short stature-pituitary and cerebellar defects-small sella turcica syndrome is characterized by short stature, anterior pituitary hormone deficiency, small sella turcica, and a hypoplastic anterior hypophysis associated with pointed cerebellar tonsils. It has been described in three generations of a large French kindred. Ectopia of the posterior hypophysis was observed in some patients. The syndrome is transmitted as a dominantly inherited trait and is caused by a germline mutation within the LIM-homeobox transcription factor LHX4 gene (1q25). Finding site True Entire sella turcica (body structure) Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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