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764992006: Muscle filaminopathy (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3655974016 Muscle filaminopathy en Synonym Active Case insensitive SNOMED CT core
3655975015 Muscle filaminopathy (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3655797013 A rare myofibrillar myopathy with characteristics of slowly progressive, proximal skeletal muscle weakness, which is initially more prominent in lower extremities and involves upper extremities with disease progression. Patients present with difficulty climbing stairs, a waddling gait, marked winging of scapula, lower back pain, paresis of limb girdle musculature, hypo or areflexia and/or mild facial muscle weakness in rare cases. Respiratory muscle weakness is common and cardiac anomalies (conduction blocks, tachycardia, diastolic dysfunction, left ventricular hypertrophy) have been reported in some cases. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Muscle filaminopathy Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Muscle filaminopathy Is a Congenital disease true Inferred relationship Some
Muscle filaminopathy Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Muscle filaminopathy Is a Myofibrillar myopathy true Inferred relationship Some
Muscle filaminopathy Occurrence Congenital true Inferred relationship Some 1
Muscle filaminopathy Finding site Skeletal muscle structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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