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774080007: Neonatal scleroderma (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. 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
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
3435591001000112 Neonatale Sklerodermie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
951671000172115 sclérodermie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
951671000172115 sclérodermie néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3435591001000112 Neonatale Sklerodermie 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
Neonatal scleroderma Is a Systemic sclerosis false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal scleroderma Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Associated morphology Fibrosis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Is a Neonatal disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal scleroderma Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Is a Neonatal dermatosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal scleroderma Is a Erythema of skin true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal scleroderma Is a Autoimmune skin disease true Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal scleroderma Finding site Skin structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Associated morphology Erythema true Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal scleroderma Occurrence Neonatal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal scleroderma Finding site Connective tissue structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal scleroderma Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal scleroderma Is a A rare autoimmune connective tissue disorder characterized by abnormal hardening of the skin and sometimes other organs. It is classified into two main forms: localized scleroderma and systemic sclerosis (SSc), the latter comprising three subsets; diffuse cutaneous SSc (dcSSc), limited cutaneous SSc (lcSSc) and limited SSc (lSSc). Localized scleroderma is the cutaneous form of scleroderma characterized by fibrosis of the skin causing cutaneous plaques (morphea) or strips (linear scleroderma). Systemic sclerosis (SSc) is a generalized disorder characterized by fibrosis and vascular obliteration in the skin and organs, particularly, lungs, heart, and digestive tract. The exact cause of scleroderma is unknown. The disease originates from an autoimmune reaction, which leads to localized overproduction of collagen. In some cases, the condition is associated with exposure to chemicals. Other suggested causes include genetic and infectious mechanisms. true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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