FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.24  |  FHIR Version n/a  User: [n/a]

237873000: Primary familial amyloid myopathy (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
356483013 Primary familial amyloid myopathy en Synonym Active Entire term case insensitive SNOMED CT core module
626664017 Primary familial amyloid myopathy (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Primary familial amyloid myopathy Is a Amyloid myopathy true Inferred relationship Existential restriction modifier
Primary familial amyloid myopathy Associated morphology Amyloid deposition false Inferred relationship Existential restriction modifier 1
Primary familial amyloid myopathy Finding site Skeletal muscle structure false Inferred relationship Existential restriction modifier 1
Primary familial amyloid myopathy Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 1
Primary familial amyloid myopathy Finding site Skeletal muscle structure 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