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62382002: Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (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
103687015 CRST syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
103689017 Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232327014 CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232328016 Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2621011013 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2838289013 Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914004011 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914070015 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
103687015 CRST syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
103689017 Calcinosis cutis, Raynaud's, sclerodactyly AND telangiectasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
801548013 CRST syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
801548013 CRST syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232327014 CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232327014 CRST - Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1232328016 Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1232329012 Calcinosis, Raynaud's phenomenon, sclerodactyly, telangiectasia syndrome (disorder) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2612522019 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2621011013 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2838289013 Calcinosis, Raynaud phenomenon, sclerodactyly, and telangiectasia (CRST) syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914004011 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2914070015 Calcinosis, Raynaud's phenomenon, sclerodactyly, and telangiectasia syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
395721000172114 syndrome de CRST fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
395721000172114 syndrome de CRST fr 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
CRST syndrome Is a Acrosclerosis false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Secondary Raynaud's phenomenon true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Vascular disease of the skin false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Calcinosis cutis true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Associated morphology Sclerosis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Finding site Structure of fascia (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Associated morphology Telangiectasis true Inferred relationship Existential restriction modifier (core metadata concept) 5
CRST syndrome Finding site Connective tissue false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
CRST syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Associated morphology Pathologic calcification false Inferred relationship Existential restriction modifier (core metadata concept) 1
CRST syndrome Finding site Structure of artery of limb false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Connective tissue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Skin structure of digit (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
CRST syndrome Associated morphology Deposition false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Is a Sclerosis of the skin false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Systemic sclerosis with limited cutaneous involvement true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Disorder of digit true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Disorder of soft tissue of limb false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Structure of collagen fibers of skin false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Is a Disorder of hand (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding method Procedure false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Interprets Body colour false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Hand structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
CRST syndrome Interprets Color of skin false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Has definitional manifestation Immune system finding false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Pathological process (attribute) Autoimmune process false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Skin structure of digit (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
CRST syndrome Associated morphology Pathologic calcification true Inferred relationship Existential restriction modifier (core metadata concept) 1
CRST syndrome Associated morphology Sclerosis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Finding site Structure of fascia (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Is a Autoimmune skin disease false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Associated morphology Fibrosis (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Associated morphology Dystrophic calcification false Inferred relationship Existential restriction modifier (core metadata concept) 2
CRST syndrome Is a Systemic disease affecting skin true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Associated morphology Fibrosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 4
CRST syndrome Finding site Connective tissue structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
CRST syndrome Pathological process (attribute) Autoimmune process true Inferred relationship Existential restriction modifier (core metadata concept) 4
CRST syndrome Is a Disorder of cardiovascular system true Inferred relationship Existential restriction modifier (core metadata concept)
CRST syndrome Finding site Peripheral vascular system structure true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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