loading...| Preferred Name |
Retinopathy of Prematurity |
| ID |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C34982 |
| ALT_DEFINITION |
A retinal condition of very immature infants that may be characterized by non-vascularized retina that may lead to neovascularization, scarring, retinal detachment, and blindness. |
| code |
C34982 |
| Concept_In_Subset |
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118466 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C189762 http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C118464 |
| Contributing_Source |
MedDRA NICHD |
| DEFINITION |
A bilateral retinopathy characterized by neovascularization, scarring, retinal detachment, and eventually blindness. It may be mild or severe. It occurs in babies born prematurely. Causes include oxygen toxicity and hypoxia. |
| FULL_SYN |
Retrolental Fibroplasia Terry Syndrome Retinopathy of Prematurity |
| label |
Retinopathy of Prematurity |
| Legacy Concept Name |
Retrolental_Fibroplasia |
| Maps_To |
Retinopathy of prematurity |
| Preferred_Name |
Retinopathy of Prematurity |
| prefixIRI |
Thesaurus:C34982 |
| prefLabel |
Retinopathy of Prematurity |
| Semantic_Type |
Disease or Syndrome |
| UMLS_CUI |
C0035344 |
| subClassOf |