MSeqDR Mitochondrial Disease Portal


 
*:HP: HPO terms, ND: NAMDC terms.
  Most Studied  CPEO, Complex I Deficiency, COXPD1, Leigh, LHON, MELAS, MERRF, NARP, SANDO
Disease Browser
Parent Node:
expandeye disease (MONDO:0005328)
Parent Node:
expandnervous system disorder (MONDO:0005071)
..Starting node
..expandretinal disease ()

       Child Nodes:
........expandangioid streaks ()
........expandautoimmune retinopathy ()
........expandcancer-associated retinopathy ()
........expandcentral serous chorioretinopathy ()
........expandEales disease ()
........expandhypertensive retinopathy ()
........expandinherited vitreous-retinal disease ()
........expandiris hypoplasia with glaucoma ()
........expandmacular holes ()
........expandmelanoma associated retinopathy ()
........expandnight blindness ()
........expandosteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome ()
........expandpseudopapilledema (disease) ()
........expandretina neoplasm ()
........expandretinal ciliopathy ()
........expandretinal degeneration ()
........expandretinal detachment ()
........expandretinal edema ()
........expandretinal ischemia ()
........expandretinal nerve fibre layer disorder ()
........expandretinal vascular disease ()
........expandretinitis ()
........expandretinopathy of prematurity ()
........expandrubeosis iridis ()



 Sister Nodes: 
..expandautoimmune disease of the nervous system ()
..expandBalint syndrome ()
..expandBarre-Lieou syndrome ()
..expandcentral nervous system disease ()
..expandcerebral disease with cataract ()
..expandcomplex neurodevelopmental disorder ()
..expandcongenital nervous system disorder ()
..expandcranial nerve neuropathy ()
..expanddevelopmental disability ()
..expanddiplegia of upper limb ()
..expanddrug-induced akathisia ()
..expanddrug-induced dyskinesia ()
..expandgenetic nervous system disorder ()
..expandGerstmann syndrome ()
..expandidiopathic recurrent stupor ()
..expandinfectious disease of the nervous system ()
..expandinherited nervous system cancer-predisposing syndrome ()
..expandlocked-in syndrome ()
..expandmovement disorder ()
..expandneonatal brainstem dysfunction ()
..expandnervous system injury ()
..expandnervous system neoplasm ()
..expandneurocutaneous syndrome ()
..expandneuroendocrine disease ()
..expandneuronitis ()
..expandneurosarcoidosis ()
..expandneurovascular disease ()
..expandpalsy ()
..expandparaneoplastic neurologic syndrome ()
..expandperceptual disorders ()
..expandperineural cyst ()
..expandperipheral nervous system disease ()
..expandpersistent idiopathic facial pain ()
..expandprimary orthostatic hypotension ()
..expandradiculitis ()
..expandrare disease with malignant hyperthermia ()
..expandrare neuroinflammatory or neuroimmunological disease ()
..expandrare neurologic disease with psychiatric involvement ()
..expandrestless legs syndrome ()
..expandretinal disease ()
..expandsensory ganglionopathy ()
..expandsleep-wake disorder ()
..expandspecific learning disability ()
..expandspontaneous periodic hypothermia ()
..expandsymmetrical thalamic calcifications ()
..expandtoxic encephalopathy ()
..expandWallerian degeneration ()
..expandWorster-Drought syndrome ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:5283
Name:retinal disease
Definition:Any disease or disorder of the retina.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:eye disease of retina; retina eye disease; retinopathy
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal