FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

721608001: Hirschsprung disease of rectosigmoid region (disorder)


Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3325569010 Hirschsprung disease of rectosigmoid region (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3325570011 Hirschsprung disease of rectosigmoid region en Synonym Active Entire term case insensitive SNOMED CT core module
3325571010 Rectosigmoid 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
Hirschsprung disease of rectosigmoid region Is a Hirschsprung's disease true Inferred relationship Existential restriction modifier
Hirschsprung disease of rectosigmoid region Finding site Parasympathetic nervous system structure false Inferred relationship Existential restriction modifier
Hirschsprung disease of rectosigmoid region Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier 3
Hirschsprung disease of rectosigmoid region Occurrence Congenital false Inferred relationship Existential restriction modifier 6
Hirschsprung disease of rectosigmoid region Finding site Rectosigmoid structure false Inferred relationship Existential restriction modifier 6
Hirschsprung disease of rectosigmoid region Occurrence Congenital false Inferred relationship Existential restriction modifier 7
Hirschsprung disease of rectosigmoid region Finding site Rectosigmoid structure false Inferred relationship Existential restriction modifier 7
Hirschsprung disease of rectosigmoid region Associated morphology Congenital hypertrophy false Inferred relationship Existential restriction modifier 6
Hirschsprung disease of rectosigmoid region Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 7
Hirschsprung disease of rectosigmoid region Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hirschsprung disease of rectosigmoid region Finding site Rectosigmoid structure true Inferred relationship Existential restriction modifier 2
Hirschsprung disease of rectosigmoid region Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 1
Hirschsprung disease of rectosigmoid region Finding site Rectosigmoid structure true Inferred relationship Existential restriction modifier 1
Hirschsprung disease of rectosigmoid region Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hirschsprung disease of rectosigmoid region Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Hirschsprung disease of rectosigmoid region Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hirschsprung disease of rectosigmoid region Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 2
Hirschsprung disease of rectosigmoid region Associated morphology Dilatation true Inferred relationship Existential restriction modifier 1
Hirschsprung disease of rectosigmoid region Is a Congenital dilatation of colon true Inferred relationship Existential restriction modifier
Hirschsprung disease of rectosigmoid region Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Hirschsprung disease of rectosigmoid region Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Hirschsprung disease of rectosigmoid region Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Hirschsprung disease of rectosigmoid region Finding site Structure of peripheral part of autonomic nervous system true Inferred relationship Existential restriction modifier 4
Hirschsprung disease of rectosigmoid region Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Hirschsprung disease of rectosigmoid region Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Hirschsprung disease of rectosigmoid region 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

Back to Start