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715630006: hyperpigmentation progressive familiale (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
1017661000172116 mélanose diffuse congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303230012 Familial progressive hyperpigmentation (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303231011 Familial progressive hyperpigmentation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303232016 Melanosis diffusa congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303233014 Melanosis universalis hereditaria en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3303234015 Universal melanosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
748071000241119 hyperpigmentation progressive familiale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
946851000172119 hyperpigmentation progressive familiale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
3303235019 Patches of hyperpigmentation in the skin, which are present at birth or in early infancy and increase in size and number with age. A rare autosomal dominant disorder. 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 progressive hyperpigmentation (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Familial progressive hyperpigmentation (disorder) est un(e) (attribut) Hereditary disorder of the integument false Inferred relationship Some
Familial progressive hyperpigmentation (disorder) est un(e) (attribut) Hereditary hypermelanosis (disorder) true Inferred relationship Some
Familial progressive hyperpigmentation (disorder) morphologie associée (attribut) mélanose (anomalie morphologique) true Inferred relationship Some 1
Familial progressive hyperpigmentation (disorder) localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 1
Familial progressive hyperpigmentation (disorder) est un(e) (attribut) Genetic disorder of skin pigmentation (disorder) false Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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