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


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

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 SNOMED CT core module
3434279010 Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3434280013 Hereditary inclusion body myopathy type 3 en Synonym Active Entire term case insensitive SNOMED CT core module
3434281012 Inclusion body myopathy type 3 en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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