Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Pseudoinflammatory Fundus Dystrophy, Finnish Type (DOID:9003601)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
corneal dystrophy +     
Aniridia 1  
band keratopathy 
Bietti crystalline corneoretinal dystrophy  
Brachymesomelia Renal Syndrome 
Chorioretinal Atrophy, Progressive Bifocal 
Congenital Corneal Opacities, Cornea Guttata, and Corectopia 
Congenital Hereditary Endothelial Dystrophy with Nail Hypoplasia 
congenital stromal corneal dystrophy  
Corneal Cerebellar Syndrome 
Corneal Dystrophy and Perceptive Deafness  
corneal endothelial dystrophy +   
Corneodermatoosseous Syndrome 
Dermochondrocorneal Dystrophy of Fran├žois 
Edict Syndrome  
epithelial and subepithelial dystrophy +   
Epithelial Recurrent Erosion Dystrophy  
epithelial-stromal TGFBI dystrophy +   
Fleck corneal dystrophy  
Ichthyosiform Erythroderma, Corneal Involvement, Deafness 
Judge Misch Wright Syndrome 
Kuster Majewski Hammerstein Syndrome 
Lisch epithelial corneal dystrophy 
macular corneal dystrophy  
Macular Corneal Dystrophy, Type II  
Macular Dystrophy, Fenestrated Sheen Type 
Macular Dystrophy, Retinal, 1, North Carolina Type 
Macular Dystrophy, Retinal, 2  
Meesmann corneal dystrophy  
Microcornea, Myopic Chorioretinal Atrophy, and Telecanthus  
Mousa Al din Al Nassar Syndrome 
O'Donnell Pappas Syndrome  
Oculodental Syndrome Rutherfurd Syndrome 
posterior amorphous corneal dystrophy 
posterior polymorphous corneal dystrophy +   
Pseudoinflammatory Fundus Dystrophy, Finnish Type  
Reis-Bucklers corneal dystrophy  
Ribbonlike Corneal Degeneration with Deafness 
Sammartino De Crecchio Syndrome 
Schnyder corneal dystrophy  
Spondyloepiphyseal Dysplasia with Punctate Corneal Dystrophy 
stromal dystrophy +   
subepithelial mucinous corneal dystrophy 
Sveinsson chorioretinal atrophy  

Exact Synonyms: Fundus dystrophy, pseudoinflammatory recessive form ;   Pseudoinflammatory fundus dystrophy ;   Pseudoinflammatory fundus dystrophy, Lavia type
Primary IDs: MESH:C535828 ;   RDO:0001152

paths to the root


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.