204739008: Hirschsprung's disease (disorder)

SNOMED CT Concept\Clinical finding\...

\Viscus structure finding\Abdominal organ finding\Bowel finding\...

\Finding of large intestine\Disorder of large intestine\...

\Motility disorder of large intestine\Hirschsprung's disease

\Congenital anomaly of large intestine\Aganglionosis of large intestine\Hirschsprung's disease

\Disorder of intestine\Congenital anomaly of intestinal tract\Congenital dilatation of intestinal tract\Hirschsprung's disease
\Disorder of intestine\Congenital anomaly of intestinal tract\Congenital anomaly of large intestine\Aganglionosis of large intestine\Hirschsprung's disease
\Disorder of intestine\Disorder of large intestine\Motility disorder of large intestine\Hirschsprung's disease
\Disorder of intestine\Disorder of large intestine\Congenital anomaly of large intestine\Aganglionosis of large intestine\Hirschsprung's disease
\Disorder of intestine\Dilatation of intestine\Congenital dilatation of intestinal tract\Hirschsprung's disease
\Disorder of intestine\Functional disorder of intestine\Motility disorder of intestine\Motility disorder of large intestine\Hirschsprung's disease
\Disorder of intestine\Intestinal autonomic neuropathy\Aganglionosis of large intestine\Hirschsprung's disease

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

313953017 Aganglionic megacolon en Synonym Active Entire term case insensitive SNOMED CT core module

313954011 Congenital aganglionic megacolon en Synonym Active Entire term case insensitive SNOMED CT core module

313955012 Aganglionosis en Synonym Active Entire term case insensitive SNOMED CT core module

313956013 HD - Hirschsprung's disease en Synonym Active Entire term case sensitive SNOMED CT core module

313957016 Hirschsprung's disease en Synonym Active Entire term case sensitive SNOMED CT core module

590006018 Hirschsprung's disease (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

2841693019 Hirschsprung disease en Synonym Active Entire term case sensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hirschsprung's disease	Is a	Congenital anomaly of large intestine	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Intestinal autonomic neuropathy	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Disorder of colon	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Finding site	Colon structure	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Finding site	Autonomic nerve structure	true	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Finding site	Parasympathetic nervous system structure	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Associated morphology	Congenital anomaly	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Finding site	Structure of large intestine	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Is a	Congenital malformation	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Associated morphology	Congenital dilatation	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Associated morphology	Congenital hypertrophy	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Is a	Congenital dilatation of intestinal tract	true	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Congenital dilatation of colon	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Associated morphology	Congenital dilatation	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Finding site	Colon structure	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Associated morphology	Congenital hypertrophy	false	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Is a	Congenital anomaly of large intestine	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Finding site	Structure of large intestine	false	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Is a	Disorder of colon	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Dilatation of intestine	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Aganglionosis of colon	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Is a	Congenital dilatation of colon	false	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Associated morphology	Congenital dilatation	false	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Finding site	Colon structure	false	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	4
Hirschsprung's disease	Associated morphology	Congenital hypertrophy	false	Inferred relationship	Existential restriction modifier	4
Hirschsprung's disease	Finding site	Colon structure	false	Inferred relationship	Existential restriction modifier	4
Hirschsprung's disease	Is a	Aganglionosis of large intestine	true	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Finding site	Large intestine part	true	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Finding site	Large intestine part	true	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Associated morphology	Congenital dilatation	false	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Associated morphology	Hypertrophy	true	Inferred relationship	Existential restriction modifier	2
Hirschsprung's disease	Associated morphology	Dilatation	true	Inferred relationship	Existential restriction modifier	1
Hirschsprung's disease	Is a	Motility disorder of large intestine	true	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease	Finding site	Structure of peripheral part of autonomic nervous system	true	Inferred relationship	Existential restriction modifier	4
Hirschsprung's disease	Is a	Congenital anomaly of the peripheral nervous system	true	Inferred relationship	Existential restriction modifier
Hirschsprung's disease	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	4
Hirschsprung's disease	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	4

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Long segment Hirschsprung's disease	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Short segment Hirschsprung's disease	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Total intestinal aganglionosis	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Aganglionosis of Auerbach's plexus	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Hirschsprung's disease NOS	Is a	False	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Mowat-Wilson syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Waardenburg Shah syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Haddad syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Goldberg Shprintzen megacolon syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Hirschsprung disease with deafness and polydactyly syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Hirschsprung disease with type D brachydactyly syndrome	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Hirschsprung disease with nail hypoplasia and dysmorphism	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Hirschsprung disease of rectosigmoid region	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Extensive aganglionosis Hirschsprung disease	Is a	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier
Soave endorectal pull-through operation for Hirschsprung's disease	Has focus	True	Hirschsprung's disease	Inferred relationship	Existential restriction modifier	3
Hirschsprung's disease NOS	Is a	False	Hirschsprung's disease	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
313953017	Aganglionic megacolon	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
313954011	Congenital aganglionic megacolon	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
313955012	Aganglionosis	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
313956013	HD - Hirschsprung's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
313957016	Hirschsprung's disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
590006018	Hirschsprung's disease (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module
2841693019	Hirschsprung disease	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module