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240086009: Myopathy with cytoplasmic inclusions (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
359692015 Myopathy with cytoplasmic inclusions en Synonym Active Case insensitive SNOMED CT core
629180012 Myopathy with cytoplasmic inclusions (disorder) en Fully specified name Active Case insensitive SNOMED CT core


7 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Myopathy with cytoplasmic inclusions Pathological process Pathological developmental process true Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Is a Congenital anomaly of skeletal muscle true Inferred relationship Some
Myopathy with cytoplasmic inclusions Is a Disorder of skeletal muscle false Inferred relationship Some
Myopathy with cytoplasmic inclusions Associated morphology Congenital anomaly false Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Occurrence Congenital false Inferred relationship Some
Myopathy with cytoplasmic inclusions Associated morphology Congenital anomaly false Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Finding site Skeletal muscle structure false Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Occurrence Congenital false Inferred relationship Some 2
Myopathy with cytoplasmic inclusions Associated morphology Developmental abnormality false Inferred relationship Some 2
Myopathy with cytoplasmic inclusions Finding site Skeletal muscle structure false Inferred relationship Some 2
Myopathy with cytoplasmic inclusions Finding site Skeletal muscle structure true Inferred relationship Some 1
Myopathy with cytoplasmic inclusions Is a Congenital myopathy with abnormal subcellular organelles false Inferred relationship Some
Myopathy with cytoplasmic inclusions Occurrence Congenital true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Inclusion body myopathy 2 Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
Desmin related myopathy with Mallory body-like inclusions Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
X-linked myopathy with excessive autophagy Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
Desmin-related myofibrillar myopathy Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some
Hereditary inclusion body myopathy type 4 Is a True Myopathy with cytoplasmic inclusions Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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