Code System Concept

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Code System Concept

Code System Concept Code	240086009
Code System Concept Name	Myopathy with cytoplasmic inclusions (disorder)
Code System Preferred Concept Name	Myopathy with cytoplasmic inclusions (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Superseded By Concept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	01/31/2002
SDO Date Created	01/31/2002
SDO Date Revised	01/31/2002
Description
Sequence

Extended Properties

No extended properties.

Concept Alternate Designations

SDO Designation ID	Concept Designation Description	Status	Designation Type	PHIN Preferred Term Flag	Code Flag
359692015	Myopathy with cytoplasmic inclusions	Active	Synonym	false	false

Associated Value Sets

Value Set Name	Version(s)
Clinical Finding (NNDSS)	2 , 1
Disease	10 , 9 , 8 , 7 , 6 , 5 , 4 , 3 , 2 , 1
Problem Value Set	3 , 2

Parent Concepts

Parent Concepts

Parent/Child (Relationship Type)

Congenital anomaly of skeletal muscle (disorder) {89886004 , SNOMED-CT } Congenital myopathy with abnormal subcellular organelles (disorder) {68186003 , SNOMED-CT } Disorder of skeletal muscle (disorder) {75047002 , SNOMED-CT }

Other Relationships

No other relationships present.

Child Concepts

Myopathy with cytoplasmic inclusions (disorder) {240086009 , SNOMED-CT }

Parent/Child (Relationship Type)

Desmin related myopathy with Mallory body-like inclusions (disorder) {715646003 , SNOMED-CT } Desmin-related myofibrillar myopathy (disorder) {770627003 , SNOMED-CT } Hereditary inclusion body myopathy type 4 (disorder) {770786001 , SNOMED-CT } Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) {724349009 , SNOMED-CT } Inclusion body myopathy 2 (disorder) {702382000 , SNOMED-CT } Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) {703544004 , SNOMED-CT } X-linked myopathy with excessive autophagy (disorder) {719815005 , SNOMED-CT }

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