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239085000: Symmetrical dyschromatosis of extremities (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
358299011 Symmetrical dyschromatosis of extremities en Synonym Active Entire term case insensitive SNOMED CT core module
358300015 Acropigmentation of Dohi en Synonym Active Only initial character case insensitive SNOMED CT core module
358301016 Reticulate acropigmentation of Dohi en Synonym Active Only initial character case insensitive SNOMED CT core module
628054017 Symmetrical dyschromatosis of extremities (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
Symmetrical dyschromatosis of extremities Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier
Symmetrical dyschromatosis of extremities Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Occurrence Congenital false Inferred relationship Existential restriction modifier
Symmetrical dyschromatosis of extremities Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Symmetrical dyschromatosis of extremities Is a Disorder of extremity false Inferred relationship Existential restriction modifier
Symmetrical dyschromatosis of extremities Finding site Skin structure of extremity false Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Symmetrical dyschromatosis of extremities Finding site Skin structure of extremity true Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Symmetrical dyschromatosis of extremities Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Symmetrical dyschromatosis of extremities Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Symmetrical dyschromatosis of extremities Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Symmetrical dyschromatosis of extremities Is a Congenital anomaly of limb true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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