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725433003: Autosomal recessive cerebellar ataxia Beauce type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3450449019 Autosomal recessive cerebellar ataxia Beauce type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450450019 Autosomal recessive cerebellar ataxia Beauce type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450451015 ARCA1 - autosomal recessive cerebellar ataxia type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403475010 A rare disorder characterized by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403476011 A rare disorder characterised by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450449019 Autosomal recessive cerebellar ataxia Beauce type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450450019 Autosomal recessive cerebellar ataxia Beauce type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3450451015 ARCA1 - autosomal recessive cerebellar ataxia type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3450452010 Disease with characteristics of slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403475010 A rare disorder characterized by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403476011 A rare disorder characterised by a slowly progressive pure cerebellar ataxia associated with dysarthria. It has been described in 53 individuals from 26 families of Canadian origin. The mode of transmission is autosomal recessive. Positional cloning has led to the identification of several gene mutations. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3391631001000110 Ataxie, autosomal-rezessive, Typ Beauce de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766821000241116 ataxie cérébelleuse autosomique récessive de type Beauce fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5766821000241116 ataxie cérébelleuse autosomique récessive de type Beauce fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3391631001000110 Ataxie, autosomal-rezessive, Typ Beauce de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia Beauce type (disorder) Finding site Cerebellar structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a Late onset cerebellar ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a Cerebellar ataxia true Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive cerebellar ataxia Beauce type (disorder) Is a Hereditary ataxia (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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