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204739008: Hirschsprung's disease (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
2841693019 Hirschsprung disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
313953017 Aganglionic megacolon en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
313954011 Congenital aganglionic megacolon en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
313955012 Aganglionosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
313956013 HD - Hirschsprung's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
313957016 Hirschsprung's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
527651000241117 maladie de Hirschsprung (trouble) fr Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
5621000172115 maladie de Hirschsprung fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
590006018 Hirschsprung's disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core


14 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hirschsprung's disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Hirschsprung's disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Hirschsprung's disease morphologie associée (attribut) hypertrophie true Inferred relationship Some 2
Hirschsprung's disease morphologie associée (attribut) dilatation true Inferred relationship Some 1
Hirschsprung's disease est un(e) (attribut) Motility disorder of large intestine true Inferred relationship Some
Hirschsprung's disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Hirschsprung's disease morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 3
Hirschsprung's disease localisation d'une constatation (attribut) Structure of peripheral part of autonomic nervous system (body structure) true Inferred relationship Some 4
Hirschsprung's disease est un(e) (attribut) anomalie congénitale du système nerveux périphérique true Inferred relationship Some
Hirschsprung's disease Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Hirschsprung's disease morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 4
Hirschsprung's disease morphologie associée (attribut) Congenital anomaly false Inferred relationship Some 1
Hirschsprung's disease localisation d'une constatation (attribut) Structure of large intestine (body structure) false Inferred relationship Some 1
Hirschsprung's disease est un(e) (attribut) Congenital anomaly of large intestine false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Intestinal autonomic neuropathy false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Disorder of colon (disorder) false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Congenital malformation false Inferred relationship Some
Hirschsprung's disease morphologie associée (attribut) Congenital dilatation (morphologic abnormality) false Inferred relationship Some 1
Hirschsprung's disease survenue (attribut) congénital false Inferred relationship Some
Hirschsprung's disease morphologie associée (attribut) Congenital hypertrophy false Inferred relationship Some 1
Hirschsprung's disease est un(e) (attribut) Congenital dilatation of intestinal tract true Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Congenital dilatation of colon false Inferred relationship Some
Hirschsprung's disease morphologie associée (attribut) Congenital dilatation (morphologic abnormality) false Inferred relationship Some 1
Hirschsprung's disease localisation d'une constatation (attribut) Colon structure false Inferred relationship Some 1
Hirschsprung's disease morphologie associée (attribut) Congenital hypertrophy false Inferred relationship Some 1
Hirschsprung's disease survenue (attribut) congénital false Inferred relationship Some
Hirschsprung's disease localisation d'une constatation (attribut) Colon structure false Inferred relationship Some 1
Hirschsprung's disease localisation d'une constatation (attribut) Autonomic nerve structure true Inferred relationship Some 3
Hirschsprung's disease localisation d'une constatation (attribut) Parasympathetic nervous system structure false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Congenital anomaly of large intestine false Inferred relationship Some
Hirschsprung's disease survenue (attribut) congénital true Inferred relationship Some 2
Hirschsprung's disease morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 2
Hirschsprung's disease localisation d'une constatation (attribut) Structure of large intestine (body structure) false Inferred relationship Some 2
Hirschsprung's disease est un(e) (attribut) Disorder of colon (disorder) false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Dilatation of intestine false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Aganglionosis of colon false Inferred relationship Some
Hirschsprung's disease est un(e) (attribut) Congenital dilatation of colon false Inferred relationship Some
Hirschsprung's disease survenue (attribut) congénital true Inferred relationship Some 3
Hirschsprung's disease morphologie associée (attribut) Congenital dilatation (morphologic abnormality) false Inferred relationship Some 3
Hirschsprung's disease localisation d'une constatation (attribut) Colon structure false Inferred relationship Some 3
Hirschsprung's disease survenue (attribut) congénital true Inferred relationship Some 4
Hirschsprung's disease morphologie associée (attribut) Congenital hypertrophy false Inferred relationship Some 4
Hirschsprung's disease localisation d'une constatation (attribut) Colon structure false Inferred relationship Some 4
Hirschsprung's disease est un(e) (attribut) Aganglionosis of large intestine (disorder) true Inferred relationship Some
Hirschsprung's disease survenue (attribut) congénital true Inferred relationship Some 1
Hirschsprung's disease localisation d'une constatation (attribut) Large intestine part true Inferred relationship Some 1
Hirschsprung's disease localisation d'une constatation (attribut) Large intestine part true Inferred relationship Some 2
Hirschsprung's disease morphologie associée (attribut) Congenital dilatation (morphologic abnormality) false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Aganglionosis of Auerbach's plexus est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Long segment Hirschsprung's disease est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Short segment Hirschsprung's disease est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Total intestinal aganglionosis est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Hirschsprung's disease NOS est un(e) (attribut) False Hirschsprung's disease Inferred relationship Some
Mowat-Wilson syndrome (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Waardenburg syndrome co-occurrent with Hirschsprung disease (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Haddad syndrome (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Goldberg Shprintzen megacolon syndrome (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Hirschsprung disease with deafness and polydactyly syndrome (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
syndrome de maladie de Hirschsprung-brachydactylie type D est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Hirschsprung disease of rectosigmoid region (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Extensive aganglionosis Hirschsprung disease (disorder) est un(e) (attribut) True Hirschsprung's disease Inferred relationship Some
Soave endorectal pull-through operation for Hirschsprung's disease a pour objet (attribut) True Hirschsprung's disease Inferred relationship Some 3

Reference Sets

Canada English language reference set (foundation metadata concept)

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

GB English

US English

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