80786002: Idiopathic acroosteolysis (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Musculoskeletal finding\Bone finding\Disorder of bone (disorder)\Acroosteolysis\Idiopathic acroosteolysis
\Musculoskeletal finding\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Acroosteolysis\Idiopathic acroosteolysis

\Disease\Disorder of body system\Disorder of musculoskeletal system (disorder)\Disorder of skeletal system\Disorder of bone (disorder)\Acroosteolysis\Idiopathic acroosteolysis
\Disease\Idiopathic disease\Idiopathic acroosteolysis

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

134002018 Idiopathic acroosteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

821984016 Idiopathic acroosteolysis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

4654571000241117 acro-ostéolyse idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Idiopathic acroosteolysis	Is a	Acroosteolysis	true	Inferred relationship	Some
Idiopathic acroosteolysis	Associated morphology	dégénérescence	false	Inferred relationship	Some	1
Idiopathic acroosteolysis	Finding site	Skin structure	false	Inferred relationship	Some	1
Idiopathic acroosteolysis	Associated morphology	dégénérescence	false	Inferred relationship	Some	1
Idiopathic acroosteolysis	Finding site	Skin structure	false	Inferred relationship	Some	1
Idiopathic acroosteolysis	Finding site	Bone structure	true	Inferred relationship	Some	1
Idiopathic acroosteolysis	Is a	Idiopathic disease	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare bone disease characterized by bone resorption affecting the distal phalanx, most commonly the terminal tuft, in the absence of a known cause. Patients present with shortening of the affected fingers or toes, associated with nail abnormalities (dystrophic or hypertrophic nails) and skin changes (such as ulceration or pigment anomalies).	Is a	True	Idiopathic acroosteolysis	Inferred relationship	Some

This concept is not in any reference sets