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loading...| Preferred Name |
Retinopathy of prematurity |
| ID |
http://www.orpha.net/ORDO/Orphanet_90050 |
| alternative_term |
ROP Retrolental fibroplasia |
| definition |
A rare retinal vasoproliferative disease affecting preterm infants characterized initially by a delay in physiologic retinal vascular development and compromised physiologic vascularity, and subsequently by aberrant angiogenesis in the form of intravitreal neovascularization. |
| definition_citation |
Orphanet |
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=90050 |
| has_age_of_onset |
Neonatal Infancy |
| has_inheritance |
Not applicable |
| hasDbXref |
ICD-10:H35.1 ICD-11:9B71.3 MedDRA:10038933 OMIM:133780 MeSH:D012178 UMLS:C0035344 |
| label |
Retinopathy of prematurity |
| notation |
ORPHA:90050 |
| part_of | |
| prefixIRI |
ORDO:Orphanet_90050 |
| prefLabel |
Retinopathy of prematurity |
| present_in |
Europe AND has_point_prevalence_range : 1-5 / 10 000 |
| treeView | |
| subClassOf |
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