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129609000: ataxie spinocérébelleuse dominante (trouble)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
124571000172118 ataxie spinocérébelleuse dominante fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)
208422017 Spinocerebellar ataxia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2147464014 Spinocerebellar ataxia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
518991000241110 ataxie spinocérébelleuse dominante (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)


60 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
ataxie spinocérébelleuse dominante morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
ataxie spinocérébelleuse dominante localisation d'une constatation (attribut) Structure of central nervous system (body structure) false Inferred relationship Some 1
ataxie spinocérébelleuse dominante morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 2
ataxie spinocérébelleuse dominante morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
ataxie spinocérébelleuse dominante interprète (attribut) Nervous system function (observable entity) false Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Spinocerebellar disease true Inferred relationship Some
ataxie spinocérébelleuse dominante localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1
ataxie spinocérébelleuse dominante est un(e) (attribut) maladie dégénérative du système nerveux central false Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) constatation à propos d'une lésion false Inferred relationship Some
ataxie spinocérébelleuse dominante localisation d'une constatation (attribut) moelle spinale (structure corporelle) true Inferred relationship Some 2
ataxie spinocérébelleuse dominante localisation d'une constatation (attribut) Structure of central nervous system (body structure) false Inferred relationship Some 1
ataxie spinocérébelleuse dominante morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
ataxie spinocérébelleuse dominante morphologie associée (attribut) dégénérescence false Inferred relationship Some 2
ataxie spinocérébelleuse dominante est un(e) (attribut) Ataxia false Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Degenerative brain disorder false Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Cerebellar degeneration false Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Hereditary cerebellar degeneration true Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Cerebellar ataxia true Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) Hereditary ataxia (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Autosomal recessive cerebellar ataxia due to STUB1 deficiency est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Adult-onset autosomal recessive cerebellar ataxia (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia due to vitamin E deficiency (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Autosomal recessive spinocerebellar ataxia, blindness, deafness syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 41 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 42 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 43 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Azorean disease est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ataxie spinocérébelleuse type 36 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 7 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 1 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 2 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 6 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 8 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 10 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 4 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Richards-Rundle syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Autosomal recessive cerebelloparenchymal disorder type 3 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 28 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ataxie spinocérébelleuse type 29 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 31 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ataxie spinocérébelleuse type 15/16 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 26 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 25 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 20 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 23 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 21 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 11 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 12 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 13 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ataxie spinocérébelleuse type 14 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 17 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
ataxie spinocérébelleuse type 18 est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 19 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 27 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 30 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 32 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 34 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 35 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 37 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 5 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
X-linked sideroblastic anemia with spinocerebellar ataxia est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
X-linked spinocerebellar ataxia type 3 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
X-linked spinocerebellar ataxia type 4 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar degeneration and corneal dystrophy syndrome (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Infantile onset spinocerebellar ataxia (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Family history of spinocerebellar ataxia (situation) constatation associée (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some 1
Spinocerebellar ataxia dysmorphism syndrome est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 40 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia type 38 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some
Spinocerebellar ataxia with axonal neuropathy type 1 (disorder) est un(e) (attribut) True ataxie spinocérébelleuse dominante Inferred relationship Some

Reference Sets

Client's clinical problems, conditions, diagnoses, symptoms, findings, complaints reference set (foundation metadata concept)

Most commonly used clinical problems, conditions, diagnoses, symptoms, findings and complaints, as interpreted by the provider reference set (foundation metadata concept)

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