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204739008: Congenital aganglionic megacolon (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
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
2841693019 Hirschsprung disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5197848014 Congenital aganglionic megacolon (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
313953017 Aganglionic megacolon en Synonym (core metadata concept) Active Only initial character case insensitive (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 Only initial character 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 Only initial character 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
590006018 Hirschsprung's disease (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
590006018 Hirschsprung's disease (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2841693019 Hirschsprung disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5197848014 Congenital aganglionic megacolon (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
384961000274111 Morbus Hirschsprung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3442511001000112 Hirschsprung-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5621000172115 maladie de Hirschsprung fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5621000172115 maladie de Hirschsprung fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
384961000274111 Morbus Hirschsprung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3442511001000112 Hirschsprung-Krankheit de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

14 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital aganglionic megacolon (disorder) Is a Congenital anomaly of large intestine (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Intestinal autonomic neuropathy (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Disorder of colon (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Finding site Parasympathetic nervous system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Associated morphology hypertrophie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Is a Congenital dilatation of intestinal tract true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Congenital dilatation of colon (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Associated morphology hypertrophie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Is a Congenital anomaly of large intestine (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Is a Disorder of colon (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Dilatation of intestine false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Aganglionosis of colon false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Is a Congenital dilatation of colon (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Associated morphology hypertrophie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Finding site Colon structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Is a Aganglionosis of large intestine (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Finding site Large intestine part true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Finding site Large intestine part true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital aganglionic megacolon (disorder) Associated morphology Dilatation true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital aganglionic megacolon (disorder) Is a Motility disorder of large intestine true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital aganglionic megacolon (disorder) Finding site Structure of peripheral part of autonomic nervous system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Is a Congenital anomaly of the peripheral nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital aganglionic megacolon (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital aganglionic megacolon (disorder) Is a Dilatation of large intestine true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Long segment Hirschsprung's disease (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Short segment Hirschsprung's disease Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Total intestinal aganglionosis (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Aganglionosis of Auerbach's plexus (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hirschsprung's disease NOS Is a False Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mowat-Wilson syndrome (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Waardenburg-Shah syndrome (WSS), also known as Waardenburg syndrome type 4 (WS4) is characterized by the association of Waardenburg syndrome (sensorineural hearing loss and pigmentary abnormalities) and Hirschsprung disease (aganglionic megacolon). Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Haddad syndrome (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Goldberg Shprintzen megacolon syndrome (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hirschsprung disease with deafness and polydactyly syndrome Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hirschsprung disease with type D brachydactyly syndrome Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hirschsprung disease-nail hypoplasia-dysmorphism syndrome is a fatal malformative disorder that is characterised by Hirschsprung disease, hypoplastic nails, distal limb hypoplasia and minor craniofacial dysmorphic features (flat facies, upward slanting palpebral fissures, narrow philtrum, narrow, high arched palate, micrognathia, low set ears with abnormal helices). Hydronephrosis has also been reported. There have been no further descriptions in the literature since 1988. Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hirschsprung disease of rectosigmoid region Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Extensive aganglionosis Hirschsprung disease (disorder) Is a True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Soave endorectal pull-through operation for Hirschsprung's disease Has focus True Congenital aganglionic megacolon (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3

This concept is not in any reference sets

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