FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

61665008: Turcot syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
102461015 Turcot syndrome en Synonym Active Case sensitive SNOMED CT core
1232237019 Turcot's syndrome en Synonym Active Case sensitive SNOMED CT core
800752016 Turcot syndrome (disorder) en Fully specified name Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Turcot syndrome Pathological process Pathological developmental process false Inferred relationship Some 2
Turcot syndrome Is a Developmental disorder false Inferred relationship Some
Turcot syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Turcot syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Turcot syndrome Is a Familial multiple polyposis syndrome true Inferred relationship Some
Turcot syndrome Finding site Structure of large intestine false Inferred relationship Some 1
Turcot syndrome Finding site Skin structure false Inferred relationship Some
Turcot syndrome Associated morphology Neoplasm false Inferred relationship Some
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Some
Turcot syndrome Associated morphology Multiple polyps false Inferred relationship Some 1
Turcot syndrome Associated morphology Congenital anomaly false Inferred relationship Some
Turcot syndrome Is a Intestinal polyposis syndrome false Inferred relationship Some
Turcot syndrome Is a Congenital anomaly of trunk false Inferred relationship Some
Turcot syndrome Is a Congenital anomaly of digestive system false Inferred relationship Some
Turcot syndrome Is a Congenital hamartosis false Inferred relationship Some
Turcot syndrome Associated morphology Multiple polyps true Inferred relationship Some 1
Turcot syndrome Finding site Structure of large intestine true Inferred relationship Some 1
Turcot syndrome Is a Congenital hamartoma false Inferred relationship Some
Turcot syndrome Occurrence Congenital false Inferred relationship Some 2
Turcot syndrome Associated morphology Hamartoma false Inferred relationship Some 2
Turcot syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Turcot syndrome Finding site Intestinal structure false Inferred relationship Some
Turcot syndrome Occurrence Congenital false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start