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716180009: Odontoma dysphagia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3304990013 Odontoma dysphagia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304991012 Odontoma dysphagia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304992017 Boder syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401245014 Odontoma-dysphagia syndrome is a malformation syndrome, characterized by odontomas (undifferentiated mass of the esophagus) and severe dysphagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401246010 Odontoma-dysphagia syndrome is a malformation syndrome, characterised by odontomas (undifferentiated mass of the oesophagus) and severe dysphagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304990013 Odontoma dysphagia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3304990013 Odontoma dysphagia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304991012 Odontoma dysphagia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3304991012 Odontoma dysphagia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3304992017 Boder syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3304993010 Odontoma-dysphagia syndrome is a malformation syndrome, with characteristics of odontomas and severe dysphagia. Less than ten cases have been reported so far. Three of the reported patients manifested multiple odontomas. Occasionally, cardiac, renal and hepatic involvement has been described. In several cases, autosomal dominant inheritance has been suspected. Currently, there are no genes associated with this condition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401245014 Odontoma-dysphagia syndrome is a malformation syndrome, characterized by odontomas (undifferentiated mass of the esophagus) and severe dysphagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5401246010 Odontoma-dysphagia syndrome is a malformation syndrome, characterised by odontomas (undifferentiated mass of the oesophagus) and severe dysphagia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3434421001000110 Odontomatose - Aorten- und Ösophagusstenose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3434421001000110 Odontomatose - Aorten- und Ösophagusstenose 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
Boder syndrome Is a Dysphagia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Finding site Upper digestive tract structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Boder syndrome Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Boder syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Boder syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Boder syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Boder syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Boder syndrome Interprets Function false Inferred relationship Existential restriction modifier (core metadata concept) 3
Boder syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Associated morphology Benign odontoma (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Boder syndrome Is a Benign neoplastic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Boder syndrome Is a Disorder of digestive system specific to fetus OR newborn true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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