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724349009: Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3434278019 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3434279010 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome en Synonym Active Case insensitive SNOMED CT core
3434280013 Hereditary inclusion body myopathy type 3 en Synonym Active Case insensitive SNOMED CT core
3434281012 Inclusion body myopathy type 3 en Synonym Active Case insensitive SNOMED CT core
3434282017 Disease characterized by congenital joint contractures (normalizing during early childhood), external ophthalmoplegia and proximal muscle weakness. In adult cases, the muscular weakness is progressive. Nineteen affected individuals have been described from one large family. The causative gene, the hereditary inclusion-body myopathy (IBM3) gene, has been mapped to chromosome region 17p13.1. Inheritance is autosomal dominant. en Definition Active Case sensitive SNOMED CT core
3434283010 Disease characterised by congenital joint contractures (normalising during early childhood), external ophthalmoplegia and proximal muscle weakness. In adult cases, the muscular weakness is progressive. Nineteen affected individuals have been described from one large family. The causative gene, the hereditary inclusion-body myopathy (IBM3) gene, has been mapped to chromosome region 17p13.1. Inheritance is autosomal dominant. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Occurrence Congenital true Inferred relationship Some 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Occurrence Congenital true Inferred relationship Some 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Inherited arthrogryposis true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Skeletal muscle structure true Inferred relationship Some 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Joint structure false Inferred relationship Some 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Associated morphology Contracture true Inferred relationship Some 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Interprets Range of joint movement true Inferred relationship Some 3
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Has interpretation Decreased true Inferred relationship Some 3
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Structure of joint region true Inferred relationship Some 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Structure of extraocular muscle true Inferred relationship Some 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Myopathy of extraocular muscles true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Interprets Movement observable true Inferred relationship Some 6
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Has interpretation Absent true Inferred relationship Some 6
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a External ophthalmoplegia true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Arthrogryposis false Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Myopathy with cytoplasmic inclusions true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Hereditary disorder of nervous system true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Is a Hereditary disorder of the visual system true Inferred relationship Some
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Structure of nervous system true Inferred relationship Some 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Eye region structure false Inferred relationship Some 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Occurrence Congenital false Inferred relationship Some 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Occurrence Congenital false Inferred relationship Some 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Associated morphology Contracture false Inferred relationship Some 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Joint structure false Inferred relationship Some 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Associated morphology Developmental abnormality false Inferred relationship Some 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome Finding site Skeletal muscle structure false Inferred relationship Some 5

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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