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774080007: Neonatal scleroderma (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3727901010 Neonatal scleroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727902015 Neonatal scleroderma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3727903013 A very rare secondary neonatal autoimmune disease with characteristics of neonatal-onset of erythematous skin lesions with a linear appearance that gradually become indurated and hyperpigmented and progressively present skin atrophy. Positive serum antibodies (in particular antinuclear antibodies and/or rheumatoid factor) may be associated. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4204411000052116 neonatal sklerodermi sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Neonatal scleroderma Is a Systemic sclerosis true Inferred relationship Some
Neonatal scleroderma Pathological process (attribute) Autoimmune process true Inferred relationship Some 1
Neonatal scleroderma Associated morphology Fibrosis true Inferred relationship Some 1
Neonatal scleroderma Occurrence Neonatal true Inferred relationship Some 1
Neonatal scleroderma Is a Neonatal disorder true Inferred relationship Some
Neonatal scleroderma Finding site Connective tissue structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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