FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

710903001: Periodontitis co-occurrent with genetic disorder (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2015. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3046614015 Periodontitis co-occurrent with genetic disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3046636017 Periodontitis co-occurrent with genetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3046708015 Periodontitis associated with genetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3046614015 Periodontitis co-occurrent with genetic disorder (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3046614015 Periodontitis co-occurrent with genetic disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3046636017 Periodontitis co-occurrent with genetic disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3046636017 Periodontitis co-occurrent with genetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3046708015 Periodontitis associated with genetic disorder en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3046708015 Periodontitis associated with genetic disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6465031000241113 parodontite concomitante d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6465041000241115 périodontite concomitante d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6465031000241113 parodontite concomitante d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6465041000241115 périodontite concomitante d'une affection génétique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Periodontitis co-occurrent with genetic disorder (disorder) Is a Periodontitis true Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with genetic disorder (disorder) Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with genetic disorder (disorder) Associated morphology inflammation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Periodontitis co-occurrent with genetic disorder (disorder) Finding site Periodontal tissues structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Periodontitis co-occurrent with genetic disorder (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Periodontal Ehlers-Danlos syndrome Is a True Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with Chédiak-Higashi syndrome Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with Cohen syndrome Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with infantile genetic agranulocytosis Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with hypophosphatasia Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with glycogen storage disease Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Periodontitis co-occurrent with Ehlers-Danlos syndrome type 4 Is a False Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
A rare genetic syndromic intellectual disability that is characterized by congenital permanent alopecia universalis, intellectual disability, psychomotor epilepsy and periodontitis (pyorrhea). Total permanent alopecia and pyorrhea are invariably concomitant while intellectual disability and psychomotor epilepsy are observed in most patients. No other abnormality of nails or skin (apart from absence of hair) has been reported. Transmission is autosomal dominant. Is a True Periodontitis co-occurrent with genetic disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start