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Inherited Retinal Dystrophy
Last uploaded:
July 10, 2019
| Acronym | HAMIDEHSGH |
| Visibility | Public |
| Description | Inherited retinal dystrophy (IRD) as one of the rare ocular diseases encompasses different types of hereditary retinal degenerations appearing by involvement of the different layers of the posterior ocular segment. In respect of the importance of the classification systems regarding the recorded history of biologic and natural sciences, there is no classification regarding the IRD diagnoses. Therefore, we aimed to present a novel classification in this regard. |
| Status | Alpha |
| Format | OWL |
| Contact | Hamideh Sabbaghi, sabbaghi.opt@gmail.com |
| Categories | Human |
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| Id | http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_6_6
http://www.semanticweb.org/hamide/ontologies/2019/3/IRD_6_6
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|---|---|
| Preferred Name | Retinitis Pigmentosa-deafness syndrome |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label | Retinitis Pigmentosa-deafness syndrome
|
|---|---|
| prefLabel | Retinitis Pigmentosa-deafness syndrome
|
| ORPHA_Code | 886
|
| OMIM | #500004
|
| subClassOf | |
| ICD | None
|
| type | |
| SNOMED | 57838006
|
| CUI | C0271097
|
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