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239088003: Dermatopathia pigmentosa reticularis (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
358304012 DPR - Dermatopathia pigmentosa reticularis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
358305013 Dermatopathia pigmentosa reticularis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628057012 Dermatopathia pigmentosa reticularis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
358304012 DPR - Dermatopathia pigmentosa reticularis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
358305013 Dermatopathia pigmentosa reticularis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
358305013 Dermatopathia pigmentosa reticularis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
628057012 Dermatopathia pigmentosa reticularis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
628057012 Dermatopathia pigmentosa reticularis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3383551001000117 Dermatopathia pigmentosa reticularis de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981811000172118 dermatopathie réticulaire pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
981811000172118 dermatopathie réticulaire pigmentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3383551001000117 Dermatopathia pigmentosa reticularis 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
Dermatopathia pigmentosa reticularis (disorder) Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier (core metadata concept)
Dermatopathia pigmentosa reticularis (disorder) Associated morphology Hyperpigmentation (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Dermatopathia pigmentosa reticularis (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Dermatopathia pigmentosa reticularis (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dermatopathia pigmentosa reticularis (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dermatopathia pigmentosa reticularis (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Dermatopathia pigmentosa reticularis (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dermatopathia pigmentosa reticularis (disorder) 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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