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763714006: naevus en tache de vin multiples familiaux (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1010031000172119 naevus flammeus multiples familiaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3643451019 Familial multiple nevi flammei (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643452014 Familial multiple naevi flammei en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643453016 Familial multiple port-wine stains en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3643454010 Familial multiple nevi flammei en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
766361000241115 naevus en tache de vin multiples familiaux (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
944191000172110 naevus en tache de vin multiples familiaux fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3643455011 A rare genetic capillary malformation characterised by dark red to purple birthmarks which manifest as flat, sharply circumscribed cutaneous lesions, typically situated in the head and neck region, in various members of a single family. The lesions grow proportionally with the individual, change in colour and often thicken with age. There is evidence that congenital capillary malformations can be caused by somatic mosaic mutation in the GNAQ gene on chromosome 9q21. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643456012 A rare genetic capillary malformation characterized by dark red to purple birthmarks which manifest as flat, sharply circumscribed cutaneous lesions, typically situated in the head and neck region, in various members of a single family. The lesions grow proportionally with the individual, change in color and often thicken with age. There is evidence that congenital capillary malformations can be caused by somatic mosaic mutation in the GNAQ gene on chromosome 9q21. 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
Familial multiple nevi flammei (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Familial multiple nevi flammei (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Familial multiple nevi flammei (disorder) est un(e) (attribut) Familial disease true Inferred relationship Some
Familial multiple nevi flammei (disorder) est un(e) (attribut) naevus flammeus true Inferred relationship Some
Familial multiple nevi flammei (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 1
Familial multiple nevi flammei (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Familial multiple nevi flammei (disorder) localisation d'une constatation (attribut) Structure of capillary of skin 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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