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722294004: Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3331478015 Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
3331479011 Autosomal dominant intermediate Charcot-Marie-Tooth disease type E en Synonym Active Initial character case insensitive SNOMED CT core
3331480014 Charcot-Marie-Tooth disease with nephropathy syndrome en Synonym Active Case sensitive SNOMED CT core
3331481013 Syndrome with the association of Charcot-Marie-Tooth disease and nephropathy. So far, around 15 cases have been described. All patients had proteinuria at onset and some patients presented with nephrotic syndrome. In the majority of cases, pathological studies revealed glomerulosclerosis. Caused by heterozygous mutation in the INF2 gene on chromosome 14q32. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Finding site Glomerulus structure true Inferred relationship Some 2
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Is a Congenital disease false Inferred relationship Some
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Is a Glomerular disease true Inferred relationship Some
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Is a Hereditary motor and sensory neuropathy true Inferred relationship Some
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Is a Hereditary nephropathy true Inferred relationship Some
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Finding site Peripheral nervous system structure true Inferred relationship Some 1
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Occurrence Congenital false Inferred relationship Some 2
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E Finding site Glomerulus structure false 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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