FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.12  |  FHIR Version n/a  User: [n/a]

402600008: Xeroderma in genetic syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1770524011 Xeroderma in genetic syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781717014 Xeroderma in genetic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Xeroderma in genetic syndrome (disorder) est un(e) (attribut) xérodermie (trouble) true Inferred relationship Some
Xeroderma in genetic syndrome (disorder) localisation d'une constatation (attribut) structure de la peau false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) morphologie associée (attribut) Papulovesicular rash false Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) est défini par la manifestation de (attribut) Abnormal keratinisation false Inferred relationship Some
Xeroderma in genetic syndrome (disorder) localisation d'une constatation (attribut) Structure of skin region false Inferred relationship Some
Xeroderma in genetic syndrome (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 3
Xeroderma in genetic syndrome (disorder) a pour interprétation (attribut) anormal true Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) interprète (attribut) Keratinization, function (observable entity) true Inferred relationship Some 1
Xeroderma in genetic syndrome (disorder) interprète (attribut) moiteur de la peau true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start