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239082002: Dyschromatosis universalis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
358293012 Dyschromatosis universalis en Synonym Active Entire term case insensitive SNOMED CT core module
358294018 Melanism en Synonym Active Entire term case insensitive SNOMED CT core module
628050014 Dyschromatosis universalis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core 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
Dyschromatosis universalis Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Existential restriction modifier
Dyschromatosis universalis Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Dyschromatosis universalis Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Dyschromatosis universalis Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Dyschromatosis universalis Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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