FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1184703009: Periodontitis due to infantile genetic agranulocytosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4662894013 Periodontitis due to infantile genetic agranulocytosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4662903010 Periodontitis due to infantile genetic agranulocytosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5014376010 Periodontitis due to Kostmann syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
6417191000241116 parodontite due à l'agranulocytose constitutionnelle infantile fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6417201000241119 périodontite due au syndrome de Kostmann fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6417211000241117 périodontite due à la neutropénie congénitale sévère de type 3 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Periodontitis due to infantile genetic agranulocytosis (disorder) Due to Congenital neutropenia false Inferred relationship Some 2
Periodontitis due to infantile genetic agranulocytosis (disorder) Finding site Periodontal tissues structure true Inferred relationship Some 1
Periodontitis due to infantile genetic agranulocytosis (disorder) Associated morphology Inflammatory morphology (morphologic abnormality) true Inferred relationship Some 1
Periodontitis due to infantile genetic agranulocytosis (disorder) Is a Periodontitis as manifestation of systemic disease (disorder) false Inferred relationship Some
Periodontitis due to infantile genetic agranulocytosis (disorder) Is a Periodontitis due to congenital neutropenia true Inferred relationship Some
Periodontitis due to infantile genetic agranulocytosis (disorder) Due to Kostmann syndrome is a rare, severe, congenital neutropenia disorder characterized by a lack of mature neutrophils (absolute neutrophil counts less than 500 cells/mm3) associated with frequent, recurrent bacterial infections (e.g. otitis media, pneumonia, sinusitis, urinary tract infections, abscesses of skin and/or liver) and increased promyelocytes in the bone marrow. Periodontal disease, as well as neurological symptoms, such as cognitive impairment, severe neurodegeneration and epilepsy, have been reported in some patients. true Inferred relationship Some 2
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start