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237683004: X-linked panhypopituitarism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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