42433008: Recurrent ulcer (morphologic abnormality)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Apr 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

70800012 Recurrent ulcer en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

779332019 Recurrent ulcer (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2507111000005112 recidiverende ulcus da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
recidiverende ulcus	Is a	Ulcer	false	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Recurrent aphthous ulcer	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
Recurrent aphthous ulcer (disorder)	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
Recidiverende mundsår	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
recidiverende nekrotiserende mukøs periadenit?	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
recidiverende nekrotiserende mukøs periadenit?	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
Recidiverende mundsår	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	1
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases.	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	3
A rare autoinflammatory syndrome with characteristics of the presence of features of relapsing polychondritis and Behcet disease in the same individual. This includes cartilage inflammation of the ears, nose, throat and rib cage as well as recurrent oral and genital ulcers respectively. Patients may also present ocular involvement (in particular anterior uveitis or scleritis), arthritis, fever, colitis, thrombophlebitis, and central nervous system vasculitis or in rare cases arterial aneurysms. Symptoms of polychondritis occur secondary to those of Behcet disease in the vast majority of cases.	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	4
Recurrent ulcer of mouth (disorder)	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	2
Aphthous ulcers of the mouth that are recurrent.	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	5
A rare genetic hematologic and intestinal disease characterized by childhood onset of bleeding tendency with epistaxis, gum bleeding, gastrointestinal bleeding, hematuria, and menorrhagia due to impaired platelet aggregation and secretion, as well as recurrent gastrointestinal ulcer. Mildly reduced levels of coagulation factor XI have been reported in addition.	Associated morphology	False	recidiverende ulcus	Inferred relationship	Some	2

Reference Sets

Concept inactivation indicator reference set

SAME AS association reference set (foundation metadata concept)