FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

702383005: Distal myopathy 2 (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
2995166014 Distal myopathy with vocal cord weakness en Synonym Active Entire term case insensitive SNOMED CT core module
2995469010 Myopathia distalis type 2 en Synonym Active Entire term case insensitive SNOMED CT core module
2995509011 Distal myopathy 2 en Synonym Active Entire term case insensitive SNOMED CT core module
2995552011 Distal myopathy 2 (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2995569013 Vocal cord and pharyngeal dysfunction with distal myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
2995696017 Matrin 3 distal myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
3791473018 MATR3-related distal myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3791474012 VCPDM - vocal cord and pharyngeal distal myopathy en Synonym Active Entire term case sensitive SNOMED CT core module
3791475013 Vocal cord and pharyngeal distal myopathy 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
Distal myopathy 2 Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Distal myopathy 2 Is a Distal muscular dystrophy true Inferred relationship Existential restriction modifier
Distal myopathy 2 Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 3
Distal myopathy 2 Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 2
Distal myopathy 2 Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 2
Distal myopathy 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Distal myopathy 2 Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Distal myopathy 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Distal myopathy 2 Is a Autosomal dominant muscular dystrophy not predominantly limb girdle false Inferred relationship Existential restriction modifier
Distal myopathy 2 Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 1
Distal myopathy 2 Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Distal myopathy 2 Finding site Skeletal muscle structure true Inferred relationship Existential restriction modifier 1
Distal myopathy 2 Occurrence Adulthood true Inferred relationship Existential restriction modifier 1
Distal myopathy 2 Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Distal myopathy 2 Clinical course Progressive true Inferred relationship Existential restriction modifier 3
Distal myopathy 2 Finding site Vocal cord structure true Inferred relationship Existential restriction modifier 2
Distal myopathy 2 Is a Chronic disease of respiratory system true Inferred relationship Existential restriction modifier
Distal myopathy 2 Is a Weakness of vocal cord true Inferred relationship Existential restriction modifier
Distal myopathy 2 Is a Disorder of vocal cord true Inferred relationship Existential restriction modifier
Distal myopathy 2 Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start