Code System Concept

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Code System Concept

Code System Concept Code	1217213004
Code System Concept Name	Idiopathic acroosteolysis of phalanx (disorder)
Code System Preferred Concept Name	Idiopathic acroosteolysis of phalanx (disorder)
Concept Status	Published
Concept Status Date	09/01/2024
Code System Name	SNOMED-CT

Concept Relationships
Concept Details

Concept Details

Code System Code	PH_SNOMED-CT
Code System OID	2.16.840.1.113883.6.96
HL7 Table 0396 Code	SCT
Superseded By Concept
SDO Concept Status	Active
SDO Concept Status Date	09/01/2022
SDO Date Created	04/30/2022
SDO Date Revised	04/30/2022
Description	A rare bone disease with characteristics of 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).
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
5035159015	Idiopathic phalangeal acro-osteolysis	Active	Synonym	false	false
5035160013	Idiopathic acroosteolysis of phalanx	Active	Synonym	false	false
5035162017	Idiopathic phalangeal acroosteolysis	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1

Parent Concepts Parent Concepts Parent/Child (Relationship Type) Disorder of digit (disorder) {128597007 , SNOMED-CT } Idiopathic acroosteolysis (disorder) {80786002 , SNOMED-CT }	Other Relationships No other relationships present.
Child Concepts No child concepts present.

Page last reviewed:June 20, 2024
Page last updated:June 20, 2024
Content source:
- Centers for Disease Control and Prevention,