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1187565005: Autosomal dominant Charcot-Marie-Tooth disease type 2Y (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4674175018 Autosomal dominant Charcot-Marie-Tooth disease type 2Y en Synonym Active Only initial character case insensitive SNOMED CT core module
4674176017 Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation en Synonym Active Only initial character case insensitive SNOMED CT core module
4674177014 Autosomal dominant Charcot-Marie-Tooth disease type 2Y (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
4674178016 Autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP (valosin containing protein) mutation 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 2Y Is a Autosomal dominant Charcot-Marie-Tooth disease type 2 true Inferred relationship Existential restriction modifier
Autosomal dominant Charcot-Marie-Tooth disease type 2Y Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 2
Autosomal dominant Charcot-Marie-Tooth disease type 2Y Finding site Nerve structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant Charcot-Marie-Tooth disease type 2Y Associated morphology Atrophy true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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