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721010003: Heart-hand syndrome type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3323028013 Heart-hand syndrome type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323029017 Heart-hand syndrome type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323030010 Atriodigital dysplasia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323031014 Tabatznik syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402563012 Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterized by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402564018 Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterised by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323028013 Heart-hand syndrome type 2 (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323028013 Heart-hand syndrome type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323029017 Heart-hand syndrome type 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323029017 Heart-hand syndrome type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323030010 Atriodigital dysplasia type 2 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3323030010 Atriodigital dysplasia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3323031014 Tabatznik syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3323032019 An extremely rare type of heart-hand syndrome. Described in two families to date, with characteristics of upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402563012 Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterized by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402564018 Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterised by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3386801001000111 Herz-Hand-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
894071000172111 syndrome cardiomélique type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
948731000172119 dysplasie atrio-digitale type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
894071000172111 syndrome cardiomélique type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
948731000172119 dysplasie atrio-digitale type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386801001000111 Herz-Hand-Syndrom Typ 2 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Heart-hand syndrome type 2 (disorder) Is a Congenital heart disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Is a Congenital anomaly of upper limb true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Is a Dysostosis true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Is a Finding of bone of upper limb true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Is a A disorder in which there is abnormal electrical activity in the heart. true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Heart-hand syndrome type 2 (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Heart-hand syndrome type 2 (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Heart-hand syndrome type 2 (disorder) Finding site Heart structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Heart-hand syndrome type 2 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 3
Heart-hand syndrome type 2 (disorder) Finding site Bone structure of upper limb (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Heart-hand syndrome type 2 (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Heart-hand syndrome type 2 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Heart-hand syndrome type 2 (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Heart-hand syndrome type 2 (disorder) Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Heart-hand syndrome type 2 (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Heart-hand syndrome type 2 (disorder) Finding site Bone structure of upper limb (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Heart-hand syndrome type 2 (disorder) Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Heart-hand syndrome type 2 (disorder) Is a Congenital dysplasia of limb (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome type 2 (disorder) Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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