OMOP Concept 4264152
Juvenile neuronal ceroid lipofuscinosis
StandardConditionSNOMED61663001Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Juvenile neuronal ceroid lipofuscinosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 136368 | Amaurotic family idiocy, juvenile type | Non-standard |
| Nebraska Lexicon | 61663001 | Juvenile neuronal ceroid lipofuscinosis | Non-standard |
| Read | F101.11 | Amaurotic familial idiocy | Non-standard |
| Read | F101200 | Spielmeyer-Vogt (Batten) disease | Non-standard |
| Read | F101211 | Batten's disease of retina | Non-standard |
Synonyms
Alternative names recorded for Juvenile neuronal ceroid lipofuscinosis across source vocabularies.
- Amaurotic idiocy juvenile type
- Amaurotic idiocy, juvenile type
- Batten-Mayou disease
- Batten-Mayou syndrome
- Batten-Spielmeyer-Vogt disease
- Cerebral lipidosis myoclonic variant
- Cerebral lipidosis, myoclonic variant
- enfermedad de Batten - Mayou
- enfermedad de Batten - Spielmeyer - Vogt
- enfermedad de Spielmeyer - Vogt
- idiotez amaurótica, tipo juvenil
- Juvenile neuronal ceroid lipofuscinosis (disorder)
- lipidosis cerebral, variante mioclónica
- lipofuscinosis ceroide neuronal juvenil
- lipofuscinosis ceroide neuronal juvenil (trastorno)
- Spielmeyer-Vogt disease
- Spielmeyer-Vogt type neuronal ceroid lipofuscinosis
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(35)Roll up to these when you need a wider cohort.
- 1Cerebral lipidosis
- 1Disorder of pigmentation
- 1Myoclonic disorder
- 1Neuronal ceroid lipofuscinosis
- 2Degenerative disorder
- 2Disease
- 2Disorder of brain
- 2Disorder of nervous system
- 2Inherited metabolic disorder of nervous system
- 2Lipid storage disease
- 2Lipofuscinosis
- 2Lysosomal storage disease
- 2Movement disorder
- 3Clinical finding
- 3Disorder of body system
- 3Disorder of head
- 3Disorder of lipid storage and metabolism
- 3Disorder of lipoprotein AND/OR lipid metabolism
- 3Disorder of lysosomal enzyme
- 3Disorder of the central nervous system
- 3Enzymopathy
- 3Finding of brain
- 3Finding of movement
- 3Hereditary disorder of nervous system
- 3Inborn error of metabolism
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