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

719513008: Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3316647019 Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3316648012 Autosomal dominant Charcot-Marie-Tooth disease type 2L en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant Charcot-Marie-Tooth disease type 2L Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier
Autosomal dominant Charcot-Marie-Tooth disease type 2L Is a Charcot-Marie-Tooth disease, type II false Inferred relationship Existential restriction modifier
Autosomal dominant Charcot-Marie-Tooth disease type 2L Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2L Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2L Finding site Nerve structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2L Is a Autosomal dominant Charcot-Marie-Tooth disease type 2 true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start