FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

1228843008: anti-p200-pemfigoïd (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5063401014 Anti-p200 pemphigoid en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5063402019 Anti-p200 pemphigoid (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
13594381000146110 anti-p200-pemfigoïd nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13594391000146112 anti-p200-pemfigoïd (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5063403012 A rare acquired subepidermal autoimmune bullous disease with characteristics of polymorphic cutaneous lesions (blisters, urticarial lesions or scars/milia) associated with immunoglobulin G deposition in the basement membrane zone. Lesions are frequently localized on extremities, trunk, palmoplantar and cephalic areas as well as mucous membranes. The disease predominantly affects elderly people. The exact etiology is unknown but may be related to laminin gamma-1, consistent with the identified characteristics of the p200 protein (an acidic non-collagenous N-linked glycoprotein localized within the lower lamina lucida outside of hemidesmosomes). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5063404018 A rare acquired subepidermal autoimmune bullous disease with characteristics of polymorphic cutaneous lesions (blisters, urticarial lesions or scars/milia) associated with immunoglobulin G deposition in the basement membrane zone. Lesions are frequently localised on extremities, trunk, palmoplantar and cephalic areas as well as mucous membranes. The disease predominantly affects elderly people. The exact aetiology is unknown but may be related to laminin gamma-1, consistent with the identified characteristics of the p200 protein (an acidic non-collagenous N-linked glycoprotein localised within the lower lamina lucida outside of hemidesmosomes). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Anti-p200 pemphigoid Is a Pemphigoid false Inferred relationship Some
Anti-p200 pemphigoid Occurrence Period of life beginning after birth and ending before death (qualifier value) true Inferred relationship Some 1
Anti-p200 pemphigoid Finding site Structure of skin and/or mucous membrane (body structure) false Inferred relationship Some 1
Anti-p200 pemphigoid Associated morphology Blister true Inferred relationship Some 1
Anti-p200 pemphigoid Pathological process (attribute) Autoimmune process true Inferred relationship Some 1
Anti-p200 pemphigoid Finding site Epidermal basement zone true Inferred relationship Some 1
Anti-p200 pemphigoid Is a Bullous pemphigoid true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start