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703544004: Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3009059013 Lower motor neuron degeneration with Paget-like bone disease en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009150010 Pagetoid amyotrophic lateral sclerosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009177018 Muscular dystrophy limb-girdle with Paget disease of bone en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009459019 Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009478019 Pagetoid neuroskeletal syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3009492013 Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3009710019 IBMPFD - Inclusion body myopathy with early onset Paget disease and frontotemporal dementia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) est un(e) (attribut) Developmental hereditary disorder true Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) est un(e) (attribut) Myopathy with cytoplasmic inclusions true Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) est un(e) (attribut) Hereditary disorder of musculoskeletal system true Inferred relationship Some
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) morphologie associée (attribut) Developmental abnormality false Inferred relationship Some 1
Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder) localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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