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


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). 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 Entire term case insensitive (core metadata concept) SNOMED CT core
3434279010 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434280013 Hereditary inclusion body myopathy type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434281012 Inclusion body myopathy type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403310014 A rare genetic neuromuscular disease characterized by early onset of proximal or generalized muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibers, marked variability in fiber size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403311013 A rare genetic neuromuscular disease characterised by early onset of proximal or generalised muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibres, marked variability in fibre size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3434278019 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434279010 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434280013 Hereditary inclusion body myopathy type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3434281012 Inclusion body myopathy type 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) 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 Entire term case sensitive (core metadata concept) SNOMED CT core
5403310014 A rare genetic neuromuscular disease characterized by early onset of proximal or generalized muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibers, marked variability in fiber size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403311013 A rare genetic neuromuscular disease characterised by early onset of proximal or generalised muscle weakness, external ophthalmoplegia with or without ptosis, and joint contractures. Hypotonia, neonatal respiratory distress necessitating ventilation, and severe dysphagia have also been reported. The disease is of variable severity and non- or slowly progressive. Patients typically remain ambulatory. Muscle biopsy may show predominance of type 1 fibres, marked variability in fibre size, increased internal nuclei, and proliferation of perimysial and endomysial connective tissue. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
567961000274115 Syndrom mit hereditärer Einschlusskörperchenmyopathie, Gelenkkontrakturen und Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
602781000274115 Einschlusskörperchenmyopathie Typ 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391271001000111 Hereditäre Einschlusskörperchenmyopathie - Gelenkkontrakturen - Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
931491000172118 syndrome héréditaire de myopathie à corps d'inclusions-contractures articulaires-ophtalmoplégie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1007811000172116 HIBM3 - hereditary inclusion body myopathy type 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
931491000172118 syndrome héréditaire de myopathie à corps d'inclusions-contractures articulaires-ophtalmoplégie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1007811000172116 HIBM3 - hereditary inclusion body myopathy type 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
567961000274115 Syndrom mit hereditärer Einschlusskörperchenmyopathie, Gelenkkontrakturen und Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
602781000274115 Einschlusskörperchenmyopathie Typ 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391271001000111 Hereditäre Einschlusskörperchenmyopathie - Gelenkkontrakturen - Ophthalmoplegie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a External ophthalmoplegia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Arthrogryposis false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Myopathy with cytoplasmic inclusions (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Nervous system structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Eye region structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Associated morphology Contracture false Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Joint structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Inherited arthrogryposis true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Joint structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Associated morphology Contracture true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Interprets Range of joint movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Has interpretation Decreased true Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Structure of joint region true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Structure of extraocular muscle true Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Is a Myopathy of extraocular muscles true Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 6
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Has interpretation Absent true Inferred relationship Existential restriction modifier (core metadata concept) 6
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Finding site Joint structure of multiple body sites (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 7
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) Associated morphology Contracture true Inferred relationship Existential restriction modifier (core metadata concept) 7

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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