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253784007: Hyperganglionosis (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
377868019 Hyperganglionosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644585019 Hyperganglionosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
377868019 Hyperganglionosis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
377868019 Hyperganglionosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
644585019 Hyperganglionosis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
644585019 Hyperganglionosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5078591000241112 syndrome de Frey fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5078591000241112 syndrome de Frey fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hyperganglionosis (disorder) Is a Congenital functional disorders of the colon true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperganglionosis (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hyperganglionosis (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hyperganglionosis (disorder) Finding site Colon structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperganglionosis (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperganglionosis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hyperganglionosis (disorder) Is a Congenital anomaly of large intestine (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hyperganglionosis (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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