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721609009: Extensive aganglionosis Hirschsprung disease (disorder)

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

Descriptions:

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

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Extensive aganglionosis Hirschsprung disease Is a Hirschsprung's disease true Inferred relationship Existential restriction modifier
Extensive aganglionosis Hirschsprung disease Finding site Parasympathetic nervous system structure false Inferred relationship Existential restriction modifier
Extensive aganglionosis Hirschsprung disease Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier 3
Extensive aganglionosis Hirschsprung disease Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Extensive aganglionosis Hirschsprung disease Finding site Large intestine part false Inferred relationship Existential restriction modifier 4
Extensive aganglionosis Hirschsprung disease Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Extensive aganglionosis Hirschsprung disease Finding site Large intestine part false Inferred relationship Existential restriction modifier 5
Extensive aganglionosis Hirschsprung disease Associated morphology Congenital hypertrophy false Inferred relationship Existential restriction modifier 4
Extensive aganglionosis Hirschsprung disease Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 5
Extensive aganglionosis Hirschsprung disease Finding site Large intestine part true Inferred relationship Existential restriction modifier 1
Extensive aganglionosis Hirschsprung disease Finding site Large intestine part true Inferred relationship Existential restriction modifier 2
Extensive aganglionosis Hirschsprung disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Extensive aganglionosis Hirschsprung disease Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Extensive aganglionosis Hirschsprung disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Extensive aganglionosis Hirschsprung disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Extensive aganglionosis Hirschsprung disease Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 2
Extensive aganglionosis Hirschsprung disease Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 1
Extensive aganglionosis Hirschsprung disease Associated morphology Dilatation true Inferred relationship Existential restriction modifier 2
Extensive aganglionosis Hirschsprung disease Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Extensive aganglionosis Hirschsprung disease Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Extensive aganglionosis Hirschsprung disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Extensive aganglionosis Hirschsprung disease Finding site Structure of peripheral part of autonomic nervous system true Inferred relationship Existential restriction modifier 4
Extensive aganglionosis Hirschsprung disease Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Extensive aganglionosis Hirschsprung disease Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 4
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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