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699256006: Timothy syndrome type 1 (disorder)


Status: current, Primitive. Date: 31-Jan 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2983304019 Long QT syndrome with syndactyly en Synonym Active Initial character case insensitive SNOMED CT core
2983535012 Timothy syndrome type 1 (disorder) en Fully specified name Active Case sensitive SNOMED CT core
2983538014 Timothy syndrome classic type en Synonym Active Case sensitive SNOMED CT core
2983544013 Timothy syndrome type 1 en Synonym Active Case sensitive SNOMED CT core
3318416013 Timothy syndrome is a multi-system disorder with characteristics of cardiac, hand, facial and neurodevelopmental features that include QT prolongation, webbed fingers and toes, flattened nasal bridge, low-set ears, small upper jaw, thin upper lip, and characteristic features of autism or autistic spectrum disorders. Timothy syndrome is caused by mutations in the CACNA1C gene. It is inherited as autosomal dominant trait. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Timothy syndrome type 1 Pathological process Pathological developmental process true Inferred relationship Some 1
Timothy syndrome type 1 Is a Congenital cardiovascular disorder false Inferred relationship Some
Timothy syndrome type 1 Occurrence Congenital true Inferred relationship Some 2
Timothy syndrome type 1 Is a Congenital long QT syndrome true Inferred relationship Some
Timothy syndrome type 1 Is a Developmental hereditary disorder true Inferred relationship Some
Timothy syndrome type 1 Is a Timothy syndrome true Inferred relationship Some
Timothy syndrome type 1 Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Timothy syndrome type 1 Occurrence Congenital false Inferred relationship Some
Timothy syndrome type 1 Finding site Structure of heart true Inferred relationship Some 2
Timothy syndrome type 1 Is a Syndactyly true Inferred relationship Some
Timothy syndrome type 1 Associated morphology Congenital abnormal fusion false Inferred relationship Some 3
Timothy syndrome type 1 Finding site Digit structure false Inferred relationship Some 3
Timothy syndrome type 1 Is a Long QT syndrome with genetic marker false Inferred relationship Some
Timothy syndrome type 1 Occurrence Congenital true Inferred relationship Some 1
Timothy syndrome type 1 Associated morphology Congenital abnormal fusion true Inferred relationship Some 1
Timothy syndrome type 1 Finding site Digit structure true Inferred relationship Some 1
Timothy syndrome type 1 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Timothy syndrome type 1 Is a Multiple system malformation syndrome false Inferred relationship Some
Timothy syndrome type 1 Is a Cardiovascular system hereditary disorder false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

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