FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dyschromatosis universalis Is a Inherited cutaneous hyperpigmentation true Inferred relationship Some
Dyschromatosis universalis Associated morphology Hyperpigmentation false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure true Inferred relationship Some 1
Dyschromatosis universalis Finding site Structure of skin region false Inferred relationship Some 1
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Some
Dyschromatosis universalis Associated morphology Congenital anomaly false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 1
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 2
Dyschromatosis universalis Occurrence Congenital false Inferred relationship Some 3
Dyschromatosis universalis Associated morphology Developmental anomaly false Inferred relationship Some 3
Dyschromatosis universalis Finding site Skin structure false Inferred relationship Some 3
Dyschromatosis universalis Occurrence Congenital true Inferred relationship Some 1
Dyschromatosis universalis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Dyschromatosis universalis Associated morphology Hyperpigmentation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start