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720637005: Charcot-Marie-Tooth disease type 2H (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3321619016 Charcot-Marie-Tooth disease type 2H (disorder) en Fully specified name Active Case sensitive SNOMED CT core
3321620010 Charcot-Marie-Tooth disease type 2H en Synonym Active Case sensitive SNOMED CT core
3321621014 Axonal Charcot-Marie-Tooth disease with pyramidal involvement en Synonym Active Initial character case insensitive SNOMED CT core
3321622019 An axonal peripheral sensorimotor polyneuropathy associated with pyramidal involvement. So far, it has been described in 13 members of a large Tunisian family. Onset occurred during the first decade of life with progressive distal atrophy involving both the upper and lower limbs, associated with a mild pyramidal syndrome (brisk patellar and upper limb reflexes, absent ankle reflexes and unattainable plantar reflexes). Transmitted in an autosomal recessive manner and the disease-causing locus has been mapped to 8q13-21.1. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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