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715727009: Pituitary stalk interruption syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3303535018 Pituitary stalk interruption syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3303536017 Pituitary stalk interruption syndrome en Synonym Active Case insensitive SNOMED CT core
3303537014 Ectopic neurohypophysis en Synonym Active Case insensitive SNOMED CT core
3303538016 A congenital abnormality of the pituitary that is responsible for pituitary deficiency with usual manifestation of a triad of very thin or interrupted pituitary stalk, an ectopic (or absent) posterior pituitary and hypoplasia or aplasia of the anterior pituitary. In the majority of cases no genetic cause is found, however, the presence of familial forms and the association with microphallus and congenital abnormalities, particularly of the eyes, suggest an antenatal origin. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pituitary stalk interruption syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Pituitary stalk interruption syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Pituitary stalk interruption syndrome Is a Congenital anomaly of pituitary gland true Inferred relationship Some
Pituitary stalk interruption syndrome Associated morphology Developmental abnormality false Inferred relationship Some 1
Pituitary stalk interruption syndrome Occurrence Congenital true Inferred relationship Some 1
Pituitary stalk interruption syndrome Finding site Pituitary stalk structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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