FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

422348008: Andersen Tawil syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2006. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2615429018 Andersen Tawil syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
2618098014 Andersen Tawil syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2985437015 Andersen cardiodysrhythmic periodic paralysis en Synonym Active Entire term case sensitive SNOMED CT core module
2985563011 Long QT syndrome 7 en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Andersen Tawil syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Conduction disorder of the heart false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Structural disorder of heart false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Is a Long QT syndrome with genetic marker false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Congenital heart disease true Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Is a Congenital anomaly of musculoskeletal system true Inferred relationship Existential restriction modifier
Andersen Tawil syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Andersen Tawil syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Andersen Tawil syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier 3
Andersen Tawil syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Andersen Tawil syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Andersen Tawil syndrome Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier 4
Andersen Tawil syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Andersen Tawil syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Finding site Structure of musculoskeletal system true Inferred relationship Existential restriction modifier 1
Andersen Tawil syndrome Is a Congenital long QT syndrome true Inferred relationship Existential restriction modifier
Andersen Tawil 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

Back to Start