OMOP Concept 35622229
Hereditary ataxia
StandardConditionSNOMED763597000Disorder
Maps from
15
Descendants
162
Valid from
31 Jul 2018
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
15 source codes normalize to Hereditary ataxia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 156595 | Hereditary ataxia | Non-standard |
| CIM10 | G11 | Hereditary ataxia | Non-standard |
| CIM10 | G11.8 | Other hereditary ataxias | Non-standard |
| ICD10 | G11 | Hereditary ataxia | Non-standard |
| ICD10 | G11.8 | Other hereditary ataxias | Non-standard |
| ICD10CM | G11 | Hereditary ataxia | Non-standard |
| ICD10CM | G11.8 | Other hereditary ataxias | Non-standard |
| ICD10CN | G11 | Hereditary ataxia | Non-standard |
| ICD10CN | G11.8 | Other hereditary ataxias | Non-standard |
| ICD10CN | G11.800 | Other hereditary ataxias | Non-standard |
| ICD10CN | G11.801 | Ataxia - clumsy hand syndrome (machine translation) | Non-standard |
| ICD10GM | G11 | Hereditary ataxia | Non-standard |
| ICD10GM | G11.8 | Other hereditary ataxias | Non-standard |
| KCD7 | G11 | Hereditary ataxia | Non-standard |
| KCD7 | G11.8 | Other hereditary ataxias | Non-standard |
Synonyms
Alternative names recorded for Hereditary ataxia across source vocabularies.
- ataxia hereditaria
- ataxia hereditaria (trastorno)
- Hereditary ataxia (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(162)Included automatically when you query with descendants.
- 1Arts syndrome
- 1Ataxia co-occurrent and due to abetalipoproteinemia
- 1Ataxia co-occurrent and due to phytanic acid storage disease
- 1Ataxia pancytopenia syndrome
- 1Ataxia with deafness and intellectual disability syndrome
- 1Ataxia with tapetoretinal degeneration syndrome
- 1Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
- 1Autosomal dominant cerebellar ataxia type 2
- 1Autosomal dominant spastic ataxia type 1
- 1Autosomal dominant spastic paraplegia type 79A
- 1Autosomal recessive ataxia due to ubiquinone deficiency
- 1Autosomal recessive cerebellar ataxia Beauce type
- 1Autosomal recessive cerebellar ataxia due to CWF19L1 deficiency
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
- 1Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
- 1Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
- 1Autosomal recessive cerebellar ataxia with late-onset spasticity
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
- 1Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
- 1Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
- 1Autosomal recessive posterior column ataxia and retinitis pigmentosa
- 1Autosomal recessive spastic ataxia of Charlevoix-Saguenay
- 1Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome
- 1Autosomal recessive spastic ataxia with leukoencephalopathy
- 1Behr syndrome
Showing 25 of 162. Retrieve the full set via the API.
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