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720637005: Charcot-Marie-Tooth disease type 2H (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
3321619016 Charcot-Marie-Tooth disease type 2H (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3321620010 Charcot-Marie-Tooth disease type 2H en Synonym Active Entire term case sensitive SNOMED CT core module
3321621014 Axonal Charcot-Marie-Tooth disease with pyramidal involvement 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
Charcot-Marie-Tooth disease type 2H Is a Autosomal recessive hereditary disorder false Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease type 2H Is a Charcot-Marie-Tooth disease, type II false Inferred relationship Existential restriction modifier
Charcot-Marie-Tooth disease type 2H Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
Charcot-Marie-Tooth disease type 2H Associated morphology Atrophy true Inferred relationship Existential restriction modifier 2
Charcot-Marie-Tooth disease type 2H Finding site Nerve structure true Inferred relationship Existential restriction modifier 2
Charcot-Marie-Tooth disease type 2H Is a Autosomal recessive 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

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