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715644000: malformation glomuveineuse (trouble)


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
1015791000172111 malformation glomuveineuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303273015 Glomuvenous malformation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303274014 Glomuvenous malformation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303275010 Hereditary multiple glomangioma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303276011 Venous malformations with glomus cells en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748141000241110 malformation glomuveineuse (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
981891000172113 glomangioma multiples héréditaires fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303277019 Hereditary vascular malformations featuring the presence of small, multifocal bluish-purple venous lesions involving the skin. May be present at birth, and slowly expand during childhood. New small lesions appear with time. Often painful on palpation and cannot be completely emptied by compression. They are usually multifocal and are located mainly on the extremities, involving the skin and subcutis. Caused by mutations in the gene encoding glomulin and inherited in an autosomal dominant manner. 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
malformation glomuveineuse morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
malformation glomuveineuse Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
malformation glomuveineuse est un(e) (attribut) Congenital venous malformation of skin (disorder) true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Arterial malformation true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Congenital abnormality of vein true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Cardiovascular system hereditary disorder true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Hereditary disorder of the integument true Inferred relationship Some
malformation glomuveineuse est un(e) (attribut) Cutaneous vascular malformation (disorder) false Inferred relationship Some
malformation glomuveineuse morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 1
malformation glomuveineuse survenue (attribut) congénital true Inferred relationship Some 1
malformation glomuveineuse localisation d'une constatation (attribut) Structure of glomus body (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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