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37650008: Hereditary cerebellar degeneration (disorder)


Status: current, 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
62802011 Hereditary cerebellar degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769541014 Hereditary cerebellar degeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


72 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary cerebellar degeneration est un(e) (attribut) Hereditary degenerative disease of central nervous system true Inferred relationship Some
Hereditary cerebellar degeneration morphologie associée (attribut) Degenerative abnormality true Inferred relationship Some 1
Hereditary cerebellar degeneration est un(e) (attribut) Primary cerebellar degeneration false Inferred relationship Some
Hereditary cerebellar degeneration est un(e) (attribut) Hereditary disorder of nervous system false Inferred relationship Some
Hereditary cerebellar degeneration est un(e) (attribut) Spinocerebellar disease false Inferred relationship Some
Hereditary cerebellar degeneration localisation d'une constatation (attribut) structure cérébelleuse true Inferred relationship Some 1
Hereditary cerebellar degeneration morphologie associée (attribut) Primary degeneration false Inferred relationship Some 1
Hereditary cerebellar degeneration est un(e) (attribut) affection cérébelleuse false Inferred relationship Some
Hereditary cerebellar degeneration est un(e) (attribut) Degenerative brain disorder false Inferred relationship Some
Hereditary cerebellar degeneration morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Hereditary cerebellar degeneration localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 1
Hereditary cerebellar degeneration morphologie associée (attribut) dégénérescence false Inferred relationship Some 1
Hereditary cerebellar degeneration est un(e) (attribut) Cerebellar degeneration true Inferred relationship Some
Hereditary cerebellar degeneration morphologie associée (attribut) Primary degeneration false Inferred relationship Some 1
Hereditary cerebellar degeneration localisation d'une constatation (attribut) structure cérébelleuse false Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Infantile cerebellar and retinal degeneration (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
atrophie cérébrale et cérébelleuse infantile avec microcéphalie postnatale progressive est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Combined oxidative phosphorylation defect type 29 est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Progressive cerebello-cerebral atrophy (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
paraplégie spastique héréditaire (trouble) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Episodic ataxia (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Myoclonic epilepsy myopathy sensory ataxia (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Huntington disease-like syndrome est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse type 36 est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 7 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 1 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 2 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 6 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 8 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 10 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 4 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Richards-Rundle syndrome (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Autosomal recessive cerebelloparenchymal disorder type 3 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 28 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse type 29 est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 31 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse type 15/16 est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 26 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 25 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 20 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 23 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 21 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 11 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 12 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 13 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse type 14 est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 17 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse type 18 est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 19 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 27 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 30 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 32 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 34 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 35 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 37 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 5 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
X-linked sideroblastic anemia with spinocerebellar ataxia est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
X-linked spinocerebellar ataxia type 3 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
X-linked spinocerebellar ataxia type 4 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar degeneration and corneal dystrophy syndrome (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Infantile onset spinocerebellar ataxia (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia dysmorphism syndrome est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 40 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Spinocerebellar ataxia type 38 (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
Complicated hereditary spastic paraplegia est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
X-linked hereditary spastic paraplegia (disorder) est un(e) (attribut) False Hereditary cerebellar degeneration Inferred relationship Some
ataxie spinocérébelleuse dominante est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder) est un(e) (attribut) True Hereditary cerebellar degeneration Inferred relationship Some

Reference Sets

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

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