OMOP Concept 4024563
Hereditary degenerative disease of central nervous system
StandardConditionSNOMED106018006Disorder
Maps from
1
Descendants
396
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Hereditary degenerative disease of central nervous system via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Read | F1z..00 | Hereditary and degenerative diseases of the central nervous system NOS | Non-standard |
Synonyms
Alternative names recorded for Hereditary degenerative disease of central nervous system across source vocabularies.
- enfermedad degenerativa hereditaria del sistema nervioso central
- enfermedad degenerativa hereditaria del sistema nervioso central (trastorno)
- Hereditary degenerative disease of central nervous system (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 1Degenerative disease of the central nervous system
- 1Hereditary disorder of nervous system
- 2Degenerative disorder
- 2Disorder of nervous system
- 2Disorder of the central nervous system
- 2Hereditary disorder by system
- 3Central nervous system finding
- 3Disease
- 3Disorder of body system
- 3Hereditary disease
- 4Clinical finding
- 4Genetic disease
Narrower concepts
(396)Included automatically when you query with descendants.
- 14H leukodystrophy
- 1Adrenoleukodystrophy
- 1Adult onset autosomal dominant leukodystrophy
- 1Aicardi Goutieres syndrome
- 1Alkaline ceramidase 3 deficiency
- 1Amyotrophic lateral sclerosis type 4
- 1Arrested hydrocephalus
- 1Atypical Krabbe disease due to saposin A deficiency
- 1Atypical pantothenate kinase associated neurodegeneration
- 1Auditory neuropathy, optic atrophy syndrome
- 1Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein
- 1Autosomal dominant Alzheimer disease due to mutation of presenilin 1
- 1Autosomal dominant Alzheimer disease due to mutation of presenilin 2
- 1Autosomal dominant late onset basal ganglia degeneration
- 1Autosomal dominant late onset Parkinson disease
- 1Autosomal dominant striatal neurodegeneration
- 1Autosomal recessive cerebral atrophy
- 1Autosomal recessive familial Parkinson disease
- 1Autosomal recessive isolated optic atrophy
- 1Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 1Behavioral variant of frontotemporal dementia
- 1Behr syndrome
- 1Brain calcification Rajab type
- 1C11ORF73-related autosomal recessive hypomyelinating leukodystrophy
- 1CAMOS syndrome
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