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:
expandneurodegenerative disease (MONDO:0005559)
..Starting node
..expandeye degenerative disease ()

       Child Nodes:
........expandaceruloplasminemia ()
........expandAlexander disease ()
........expandautosomal dominant cerebellar ataxia ()
........expandautosomal dominant optic atrophy ()
........expandautosomal recessive cerebellar ataxia ()
........expandautosomal recessive optic atrophy ()
........expandautosomal recessive optic atrophy, OPA7 type ()
........expandblind hypertensive eye ()
........expandChediak-Higashi syndrome ()
........expandchoroidal sclerosis ()
........expandCockayne syndrome ()
........expandcorneal-cerebellar syndrome ()
........expanddeafness dystonia syndrome ()  LSDB  L: 00113;
........expanddegenerative myopia ()
........expanddystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities ()
........expandearly-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome ()
........expandearly-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome ()
........expandeyelid degenerative disease ()
........expandfatty acid hydroxylase-associated neurodegeneration ()
........expandglaucomatous atrophy of optic disc ()
........expandhereditary spastic paraplegia 2 ()
........expandhereditary spastic paraplegia 7 ()  LSDB  L: 00497;
........expandhereditary spastic paraplegia 9A ()
........expandinfantile cerebellar-retinal degeneration ()  LSDB  L: 00108;
........expandinfantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome ()
........expandKrabbe disease ()
........expandKufor-Rakeb syndrome ()
........expandLeber hereditary optic neuropathy ()  LSDB  L: 00072;
........expandmicrophthalmia-brain atrophy syndrome ()
........expandmultiple mitochondrial dysfunctions syndrome 4 ()  LSDB  L: 00530;
........expandmuscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome ()
........expandneurodegeneration with brain iron accumulation 4 ()  LSDB  L: 00422;
........expandneuronal ceroid lipofuscinosis ()
........expandoptic atrophy 2 ()
........expandosteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome ()
........expandpantothenate kinase-associated neurodegeneration ()
........expandPEHO syndrome ()
........expandPelizaeus-Merzbacher disease ()
........expandprogressive supranuclear palsy ()
........expandpsychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome ()
........expandSandhoff disease ()
........expandspastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder ()
........expandTay-Sachs disease ()
........expandtremor-ataxia-central hypomyelination syndrome ()
........expandvitreous syneresis ()



 Sister Nodes: 
..expandamyotrophic lateral sclerosis ()
..expandbrachial amyotrophic diplegia ()
..expandcerebellar degeneration ()
..expandcerebral degeneration ()
..expandcorticobasal degeneration disorder ()
..expanddemyelinating disease ()
..expandeye degenerative disease ()
..expandinherited neurodegenerative disorder ()
..expandMarchiafava-Bignami disease ()
..expandneuroaxonal dystrophy ()
..expandneurodegenerative disease with chorea ()
..expandneurodegenerative disease with dementia ()
..expandolivopontocerebellar atrophy ()
..expandoptic atrophy ()
..expandprimary progressive apraxia of speech ()
..expandsecondary Parkinson disease ()
..expandsenile degeneration of brain ()
..expandsynucleinopathy ()
..expandtauopathy ()
   

MONDO is developed by the Monarch Initiative. Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
Term ID:4884
Name:eye degenerative disease
Definition:A neurodegenerative disease that involves the eye.
Alternative IDs:
ParentIDs:
TreeNumbers:
Synonyms:degenerative disorder of eye; degenerative disorder of globe; eye neurodegenerative disease; eyeball of camera-type eye neurodegenerative disease; neurodegenerative disease of eyeball of camera-type eye
Slim Mappings:
Reference: MedGen:
MeSH:
OMIM:
MSeqDR LSDB:  
Genes:
Phenotypes
Disease Causing ClinVar Variants
MSeqDR Portal