Link to this page
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 |
No views of HAMIDEHSGH available
Jump to:
| Id | http://www.semanticweb.org/hamide/ontologies/2019/3/untitled-ontology-14#IRD_6_72
http://www.semanticweb.org/hamide/ontologies/2019/3/untitled-ontology-14#IRD_6_72
|
|---|---|
| Preferred Name | Neuronal ceroid lipofuscinosis |
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label | Neuronal ceroid lipofuscinosis
|
|---|---|
| prefLabel | Neuronal ceroid lipofuscinosis
|
| ORPHA_Code | 216
|
| OMIM | None
|
| prefixIRI | IRD_6_72
|
| subClassOf | |
| ICD | 5C56.1
|
| type | |
| SNOMED | 42012007
|
| CUI | C0027877
|
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |
- Problem retrieving properties:
Notes
Filter: