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239082002: Dyschromatosis universalis (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
358293012 Dyschromatosis universalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
358294018 Melanism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628050014 Dyschromatosis universalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
358293012 Dyschromatosis universalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358293012 Dyschromatosis universalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
358294018 Melanism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358294018 Melanism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628050014 Dyschromatosis universalis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
628050014 Dyschromatosis universalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3386351001000115 Dyschromatosis universalis hereditaria de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5027231000241112 Dyschromatose universalis fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5027231000241112 Dyschromatose universalis fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3386351001000115 Dyschromatosis universalis hereditaria de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dyschromatosis universalis Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier (core metadata concept)
Dyschromatosis universalis Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Dyschromatosis universalis Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dyschromatosis universalis Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dyschromatosis universalis Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dyschromatosis universalis Associated morphology Hyperpigmentation (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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