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260370003: Decrease (qualifier value)


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
387910013 Decrease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
652119019 Decrease (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
387910013 Decrease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
387910013 Decrease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
652119019 Decrease (qualifier value) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
652119019 Decrease (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
102221000077113 diminution fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
102221000077113 diminution fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Decrease Is a Degree findings true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Diabetic hand syndrome Has interpretation True Decrease Inferred relationship Existential restriction modifier (core metadata concept) 3
Diabetic hand syndrome due to type 2 diabetes mellitus Has interpretation True Decrease Inferred relationship Existential restriction modifier (core metadata concept) 2
Cheiroarthropathy due to diabetes mellitus type 1 (disorder) Has interpretation True Decrease Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare mitochondrial disease characterised by a highly variable phenotypic spectrum comprising delayed motor development, peripheral neuropathy, cataract, short stature due to growth hormone deficiency, nystagmus, sensorineural hearing loss, dysmorphic facial features, and skeletal abnormalities consistent with spondyloepimetaphyseal dysplasia. Hyperextensible joints, achalasia, and telangiectasia have also been described. Cognition is normal. Atrophy of the pituitary gland has been observed in brain imaging. Has interpretation True Decrease Inferred relationship Existential restriction modifier (core metadata concept) 3

This concept is not in any reference sets

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