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765745007: Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3659550018 Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3659551019 Autosomal dominant intermediate Charcot-Marie-Tooth disease type B 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 intermediate Charcot-Marie-Tooth disease type B Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Is a Hereditary motor and sensory neuropathy true Inferred relationship Existential restriction modifier
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Finding site Peripheral nervous system structure false Inferred relationship Existential restriction modifier 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Is a Congenital disease false Inferred relationship Existential restriction modifier
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Occurrence Congenital false Inferred relationship Existential restriction modifier 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B Finding site Peripheral nervous system structure 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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