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721609009: Extensive aganglionosis Hirschsprung disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3325572015 Extensive aganglionosis Hirschsprung disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3325573013 Extensive aganglionosis Hirschsprung disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Extensive aganglionosis Hirschsprung disease (disorder) Is a Congenital aganglionic megacolon true Inferred relationship Some
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Parasympathetic nervous system structure false Inferred relationship Some
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Autonomic nerve structure true Inferred relationship Some 3
Extensive aganglionosis Hirschsprung disease (disorder) Occurrence Congenital true Inferred relationship Some 4
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Large intestine part false Inferred relationship Some 4
Extensive aganglionosis Hirschsprung disease (disorder) Occurrence Congenital false Inferred relationship Some 5
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Large intestine part false Inferred relationship Some 5
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Congenital hypertrophy false Inferred relationship Some 4
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Congenital dilatation false Inferred relationship Some 5
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Large intestine part true Inferred relationship Some 1
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Large intestine part true Inferred relationship Some 2
Extensive aganglionosis Hirschsprung disease (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Extensive aganglionosis Hirschsprung disease (disorder) Occurrence Congenital true Inferred relationship Some 2
Extensive aganglionosis Hirschsprung disease (disorder) Occurrence Congenital true Inferred relationship Some 1
Extensive aganglionosis Hirschsprung disease (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Congenital dilatation false Inferred relationship Some 2
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Hypertrophy true Inferred relationship Some 1
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Dilatation true Inferred relationship Some 2
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Extensive aganglionosis Hirschsprung disease (disorder) Occurrence Congenital true Inferred relationship Some 3
Extensive aganglionosis Hirschsprung disease (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Extensive aganglionosis Hirschsprung disease (disorder) Finding site Structure of peripheral part of autonomic nervous system (body structure) true Inferred relationship Some 4
Extensive aganglionosis Hirschsprung disease (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Extensive aganglionosis Hirschsprung disease (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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