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239085000: Symmetrical dyschromatosis of extremities (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
358299011 Symmetrical dyschromatosis of extremities en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
358300015 Acropigmentation of Dohi en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358301016 Reticulate acropigmentation of Dohi en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
628054017 Symmetrical dyschromatosis of extremities (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
358299011 Symmetrical dyschromatosis of extremities en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358299011 Symmetrical dyschromatosis of extremities en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
358300015 Acropigmentation of Dohi en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358301016 Reticulate acropigmentation of Dohi en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
628054017 Symmetrical dyschromatosis of extremities (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
628054017 Symmetrical dyschromatosis of extremities (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3424451001000118 Dyschromatosis symmetrica hereditaria de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5027251000241116 dyschromatose symétrique des extrémités fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5027251000241116 dyschromatose symétrique des extrémités fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3424451001000118 Dyschromatosis symmetrica 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
Symmetrical dyschromatosis of extremities Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier (core metadata concept)
Symmetrical dyschromatosis of extremities Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Symmetrical dyschromatosis of extremities Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Symmetrical dyschromatosis of extremities Is a Disorder of limb false Inferred relationship Existential restriction modifier (core metadata concept)
Symmetrical dyschromatosis of extremities Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Symmetrical dyschromatosis of extremities Finding site Skin structure of extremity true Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Associated morphology Hyperpigmentation (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Symmetrical dyschromatosis of extremities Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Symmetrical dyschromatosis of extremities Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Symmetrical dyschromatosis of extremities Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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