OMOP Concept 253482
Cortical blindness
StandardConditionSNOMED68574006Disorder
Maps from
7
Descendants
7
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
7 source codes normalize to Cortical blindness via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 119789 | Disorder of Visual Cortex Associated with Cortical Blindness | Non-standard |
| ICD10CM | H47.61 | Cortical blindness | Non-standard |
| ICD10CM | H47.619 | Cortical blindness, unspecified side of brain | Non-standard |
| ICD9CM | 377.75 | Cortical blindness | Non-standard |
| MeSH | D019575 | Blindness, Cortical | Non-standard |
| Nebraska Lexicon | 68574006 | Cortical blindness | Non-standard |
| Read | F4H7300 | Cortical blindness | Non-standard |
Synonyms
Alternative names recorded for Cortical blindness across source vocabularies.
- ceguera cortical
- ceguera cortical (trastorno)
- Cortical blindness (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Blindness AND/OR vision impairment level
- 1Disorder of visual cortex
- 2Disorder of cerebral cortex
- 2Visual disturbance
- 2Visual system disorder
- 3Disorder of body system
- 3Disorder of brain
- 3Disorder of vision
- 3Eye / vision finding
- 3Finding of head region
- 4Clinical finding
- 4Disease
- 4Disorder of head
- 4Disorder of the central nervous system
- 4Finding of brain
- 4Head finding
- 5Central nervous system finding
- 5Disorder of nervous system
Narrower concepts
(7)Included automatically when you query with descendants.
- 1Cortical blindness, intellectual disability, polydactyly syndrome
- 1Cortical blindness of left side of brain
- 1Cortical blindness of right side of brain
- 1Early-onset epileptic encephalopathy, cortical blindness, intellectual disability, facial dysmorphism syndrome
- 1Progressive microcephaly, seizures, cortical blindness, developmental delay syndrome
- 2Bilateral cortical blindness of brain
- 2Progressive microcephaly, seizures, cortical blindness, developmental delay with combined immunodeficiency due to DIAPH1 mutation
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