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61665008: Turcot syndrome (disorder)


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
102461015 Turcot syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
800752016 Turcot syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
1232237019 Turcot's 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
Turcot syndrome Is a Intestinal polyposis syndrome false Inferred relationship Existential restriction modifier
Turcot syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier
Turcot syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier
Turcot syndrome Is a Congenital hamartosis false Inferred relationship Existential restriction modifier
Turcot syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier
Turcot syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Turcot syndrome Is a Familial multiple polyposis syndrome true Inferred relationship Existential restriction modifier
Turcot syndrome Finding site Structure of large intestine false Inferred relationship Existential restriction modifier 1
Turcot syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier
Turcot syndrome Associated morphology Neoplasm false Inferred relationship Existential restriction modifier
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier
Turcot syndrome Associated morphology Multiple polyps false Inferred relationship Existential restriction modifier 1
Turcot syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier
Turcot syndrome Associated morphology Multiple polyps true Inferred relationship Existential restriction modifier 1
Turcot syndrome Finding site Structure of large intestine true Inferred relationship Existential restriction modifier 1
Turcot syndrome Is a Congenital hamartoma false Inferred relationship Existential restriction modifier
Turcot syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier 2
Turcot syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Turcot syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Turcot syndrome Is a Developmental disorder false Inferred relationship Existential restriction modifier
Turcot syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Turcot syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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