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

237873000: Primary familial amyloid myopathy (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
356483013 Primary familial amyloid myopathy en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
626664017 Primary familial amyloid myopathy (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
Primary familial amyloid myopathy morphologie associée (attribut) Amyloid deposition true Inferred relationship Some 1
Primary familial amyloid myopathy localisation d'une constatation (attribut) structure de muscle squelettique true Inferred relationship Some 1
Primary familial amyloid myopathy morphologie associée (attribut) Amyloid deposition false Inferred relationship Some 1
Primary familial amyloid myopathy localisation d'une constatation (attribut) structure de muscle squelettique false Inferred relationship Some 1
Primary familial amyloid myopathy est un(e) (attribut) Amyloid myopathy true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start