FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1264397009: Family history of scleroderma (situation)

Status: current, 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
5172531013 Family history of scleroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172532018 Family history of scleroderma (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172531013 Family history of scleroderma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5172532018 Family history of scleroderma (situation) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Family history of scleroderma Is a FH: Autoimmune disease true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of scleroderma Is a Family history of connective tissue disorder (situation) true Inferred relationship Existential restriction modifier (core metadata concept)
Family history of scleroderma Associated finding 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) 1
Family history of scleroderma Finding context Known present (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of scleroderma Subject relationship context Person in the family true Inferred relationship Existential restriction modifier (core metadata concept) 1
Family history of scleroderma Temporal context (attribute) Current or past (actual) (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Family history of localised scleroderma Is a True Family history of scleroderma Inferred relationship Existential restriction modifier (core metadata concept)
Family history of systemic sclerosis (situation) Is a True Family history of scleroderma Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start