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237683004: X-linked panhypopituitarism (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356226017 Panhypopituitarism - X-linked en Synonym Active Initial character case insensitive SNOMED CT core
4637473017 X-linked panhypopituitarism (disorder) en Fully specified name Active Case sensitive SNOMED CT core
4637474011 X-linked panhypopituitarism en Synonym Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Panhypopituitarism - X-linked Is a X-linked hereditary disease true Inferred relationship Some
Panhypopituitarism - X-linked Is a Hereditary disorder of endocrine system true Inferred relationship Some
Panhypopituitarism - X-linked Is a Hereditary disorder of nervous system true Inferred relationship Some
Panhypopituitarism - X-linked Finding site Adenohypophysis structure true Inferred relationship Some 1
Panhypopituitarism - X-linked Interprets Pituitary hormone false Inferred relationship Some
Panhypopituitarism - X-linked Interprets Decreased hormone secretion false Inferred relationship Some
Panhypopituitarism - X-linked Finding site Pars anterior of pituitary gland false Inferred relationship Some
Panhypopituitarism - X-linked Finding site Entire endocrine gonad false Inferred relationship Some
Panhypopituitarism - X-linked Is a Panhypopituitarism true Inferred relationship Some

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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