OMOP Concept 4034961
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus
StandardConditionSNOMED237611007Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562774 | Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus | Non-standard |
| Nebraska Lexicon | 237611007 | Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus | Non-standard |
Synonyms
Alternative names recorded for Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus across source vocabularies.
- atrofia muscular, ataxia, retinitis pigmentosa y diabetes mellitus
- atrofia muscular, ataxia, retinitis pigmentosa y diabetes mellitus (trastorno)
- Furukawa Takagi Nakao syndrome
- Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus (disorder)
- síndrome de Furukawa Takagi Nakao
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(50)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Degeneration of retina
- 1Diabetes mellitus associated with genetic syndrome
- 1Hereditary ataxia
- 1Hereditary disorder of endocrine system
- 1Hereditary disorder of musculoskeletal system
- 1Hereditary disorder of the visual system
- 1Muscle atrophy
- 2Ataxia
- 2Autosomal hereditary disorder
- 2Degenerative disorder of eye
- 2Degenerative disorder of muscle
- 2Degenerative disorder of musculoskeletal system
- 2Disorder of endocrine system
- 2Disorder of musculoskeletal system
- 2Disorder of skeletal muscle
- 2Hereditary disorder by system
- 2Hereditary disorder of nervous system
- 2Retinal disorder
- 2Secondary diabetes mellitus
- 2Visual system disorder
- 3Anomaly of eye
- 3Degenerative disorder
- 3Diabetes mellitus
- 3Disorder of body system
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