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770759001: Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3702487015 Autosomal dominant intermediate Charcot-Marie-Tooth disease type F en Synonym Active Only initial character case insensitive SNOMED CT core module
3702488013 Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (disorder) en Fully specified name 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 F Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F Finding site Peripheral nervous system structure true Inferred relationship Existential restriction modifier 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F Is a Hereditary motor and sensory neuropathy 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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