OMOP Concept 37472233
Neuronal ceroid lipofuscinosis type 11
StandardConditionSNOMED1373775000Disorder
Maps from
0
Descendants
0
Valid from
1 Oct 2025
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Neuronal ceroid lipofuscinosis type 11 across source vocabularies.
- enfermedad LCN11
- LCN11 - lipofuscinosis ceroide neuronal tipo 11
- lipofuscinosis ceroidea neuronal tipo 11
- lipofuscinosis ceroide neuronal tipo 11
- lipofuscinosis ceroide neuronal tipo 11 (trastorno)
- NCL11 - neuronal ceroid lipofuscinosis type 11
- Neuronal ceroid lipofuscinosis type 11 (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(61)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Cerebellar ataxia
- 1Hereditary ataxia
- 1Hereditary cerebellar atrophy
- 1Hereditary disorder of the visual system
- 1Neuronal ceroid lipofuscinosis
- 1Retinal dystrophy
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Cerebellar disorder
- 2Chronic brain syndrome
- 2Chronic metabolic disorder
- 2Degeneration of retina
- 2Degenerative brain disorder
- 2Hereditary cerebellar degeneration
- 2Hereditary degenerative disease of central nervous system
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Inherited metabolic disorder of nervous system
- 2Lipofuscinosis
- 2Lysosomal storage disease
- 2Visual system disorder
- 3Cerebellar degeneration
- 3Chronic disease
- 3Chronic nervous system disorder
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