OMOP Concept 4035184
Atrophia bulborum hereditaria
StandardConditionSNOMED15228007Disorder
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 Atrophia bulborum hereditaria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 148189 | Atrophia bulborum hereditaria | Non-standard |
| MeSH | C537849 | Norrie disease | Non-standard |
Synonyms
Alternative names recorded for Atrophia bulborum hereditaria across source vocabularies.
- atrofia bulborum hereditaria
- Atrophia bulborum hereditaria (disorder)
- enfermedad de Norrie
- enfermedad de Norrie (trastorno)
- Norrie's disease
- oligofrenia microftalmía
- Oligophrenia microphthalmus
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(29)Roll up to these when you need a wider cohort.
- 1Atrophic retina
- 1Hereditary disorder of the visual system
- 1X-linked recessive hereditary disease
- 2Atrophy of globe of eye
- 2Degeneration of retina
- 2Hereditary disorder by system
- 2Visual system disorder
- 2X-linked hereditary disease
- 3Degenerative disorder of eye
- 3Disorder of body system
- 3Eye / vision finding
- 3Hereditary disease
- 3Retinal disorder
- 3Sex-linked hereditary disorder
- 4Anomaly of eye
- 4Clinical finding
- 4Degenerative disorder
- 4Disease
- 4Disorder of vitreous body and/or retina
- 4Genetic disease
- 4Retina finding
- 5Disorder of eye
- 5Disorder of posterior segment of eye
- 5Globe finding
- 6Disorder of eye region
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