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783737007: Hirschsprung disease, ganglioneuroblastoma syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3760094010 Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3760095011 Hirschsprung disease, ganglioneuroblastoma syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hirschsprung disease, ganglioneuroblastoma syndrome Is a Neoplastic disease true Inferred relationship Existential restriction modifier
Hirschsprung disease, ganglioneuroblastoma syndrome Is a Congenital anomaly of large intestine true Inferred relationship Existential restriction modifier
Hirschsprung disease, ganglioneuroblastoma syndrome Is a Genetic disease true Inferred relationship Existential restriction modifier
Hirschsprung disease, ganglioneuroblastoma syndrome Finding site Large intestine part true Inferred relationship Existential restriction modifier 1
Hirschsprung disease, ganglioneuroblastoma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Hirschsprung disease, ganglioneuroblastoma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hirschsprung disease, ganglioneuroblastoma syndrome Finding site Large intestine part true Inferred relationship Existential restriction modifier 2
Hirschsprung disease, ganglioneuroblastoma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hirschsprung disease, ganglioneuroblastoma syndrome Associated morphology Dilatation true Inferred relationship Existential restriction modifier 1
Hirschsprung disease, ganglioneuroblastoma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hirschsprung disease, ganglioneuroblastoma syndrome Is a Autonomic neuropathy true Inferred relationship Existential restriction modifier
Hirschsprung disease, ganglioneuroblastoma syndrome Is a Congenital dilatation of intestinal tract true Inferred relationship Existential restriction modifier
Hirschsprung disease, ganglioneuroblastoma syndrome Associated morphology Hypertrophy true Inferred relationship Existential restriction modifier 2
Hirschsprung disease, ganglioneuroblastoma syndrome Finding site Autonomic nerve structure true Inferred relationship Existential restriction modifier 4
Hirschsprung disease, ganglioneuroblastoma syndrome Associated morphology Neuroepitheliomatous neoplasm true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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