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63135006: Amyotonia congenita (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
104952014 Amyotonia congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
104953016 Oppenheim's disease en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
104954010 Congenital atonic pseudoparalysis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499491010 Oppenheim's amyotonia en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
802385015 Amyotonia congenita (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Amyotonia congenita Is a Disorder of neuromuscular transmission true Inferred relationship Some
Amyotonia congenita Is a Myopathy false Inferred relationship Some
Amyotonia congenita Finding site Skeletal muscle structure false Inferred relationship Some
Amyotonia congenita Finding site Peripheral nervous system structure false Inferred relationship Some
Amyotonia congenita Is a Disorder of skeletal muscle false Inferred relationship Some
Amyotonia congenita Finding site Neuromuscular junction (cell structure) false Inferred relationship Some
Amyotonia congenita Is a Myoneural disorder true Inferred relationship Some
Amyotonia congenita Is a Disorder of skeletal muscle false Inferred relationship Some
Amyotonia congenita Occurrence Congenital true Inferred relationship Some 2
Amyotonia congenita Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Amyotonia congenita Occurrence Congenital true Inferred relationship Some 1
Amyotonia congenita Is a Hereditary disorder of nervous system true Inferred relationship Some
Amyotonia congenita Is a Congenital disease (disorder) true Inferred relationship Some
Amyotonia congenita Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Amyotonia congenita Finding site Neuromuscular junction (cell structure) true Inferred relationship Some 2
Amyotonia congenita Finding site Skeletal muscle structure 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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