FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

1217213004: Idiopathic acroosteolysis of phalanx (disorder)


Status: current, 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
5399916016 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). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399917013 A rare bone disease characterised 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). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5035159015 Idiopathic phalangeal acro-osteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5035160013 Idiopathic acroosteolysis of phalanx en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5035161012 Idiopathic acroosteolysis of phalanx (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5035162017 Idiopathic phalangeal acroosteolysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
7752671000241111 acro-ostéolyse phalangienne idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3409711001000116 Akroosteolyse, idiopathische phalangeale de 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
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 Disorder of digit true Inferred relationship Some
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 Idiopathic acroosteolysis true Inferred relationship Some
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). Finding site Structure of distal phalanx (body structure) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

Back to Start