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702349003: Actin accumulation myopathy (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
2995200014 Actin accumulation myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995370010 Nemaline myopathy 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995468019 Actin accumulation myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995863016 Congenital myopathy with excess thin filaments en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995200014 Actin accumulation myopathy (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995200014 Actin accumulation myopathy (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995370010 Nemaline myopathy 3 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995370010 Nemaline myopathy 3 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995468019 Actin accumulation myopathy en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995468019 Actin accumulation myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2995863016 Congenital myopathy with excess thin filaments en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2995863016 Congenital myopathy with excess thin filaments en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3428021001000112 Myopathie, kongenitale, mit Exzess dünner Filamente de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5448761000241116 myopathie avec surcharge en actine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5448761000241116 myopathie avec surcharge en actine fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3428021001000112 Myopathie, kongenitale, mit Exzess dünner Filamente 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
Actin accumulation myopathy (disorder) Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Actin accumulation myopathy (disorder) Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier (core metadata concept)
Actin accumulation myopathy (disorder) Finding site Structure of musculoskeletal system false Inferred relationship Existential restriction modifier (core metadata concept) 1
Actin accumulation myopathy (disorder) Is a Nemaline myopathy, early onset type true Inferred relationship Existential restriction modifier (core metadata concept)
Actin accumulation myopathy (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Actin accumulation myopathy (disorder) Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Actin accumulation myopathy (disorder) Is a Autosomal hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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