FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

61665008: Turcot syndrome (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
102461015 Turcot syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
800752016 Turcot syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232237019 Turcot's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
102461015 Turcot syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
800752016 Turcot syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
800752016 Turcot syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232237019 Turcot's syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232237019 Turcot's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4592251000241119 syndrome de Turcot fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4592251000241119 syndrome de Turcot fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Turcot syndrome Is a Intestinal polyposis syndrome (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Is a Congenital anomaly of trunk false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Is a Congenital anomaly of digestive system false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Is a Hamartomatous disease false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Finding site Intestinal structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Is a Familial multiple polyposis syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Finding site Structure of large intestine (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turcot syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Associated morphology Neoplasm false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Associated morphology Multiple polyps false Inferred relationship Existential restriction modifier (core metadata concept) 1
Turcot syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Associated morphology Multiple polyps true Inferred relationship Existential restriction modifier (core metadata concept) 1
Turcot syndrome Finding site Structure of large intestine (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Turcot syndrome Is a Congenital hamartoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turcot syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Turcot syndrome Is a Developmental disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Turcot syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Turcot syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start