Details of Disease

General Information of Disease (ID: DIS8R6NJ)

Disease Name Vision disorder
Synonyms visual Field disorder; visual system disorder; disorder of visual system; visual disorder; disorder of vision; vision disorder
Definition Any impairment to the vision.
Disease Hierarchy
DISH7H5I: Human disease
DISQ1B1S: Disorder of visual system
DISHEDII: Perceptual disorders
DIS8R6NJ: Vision disorder
Disease Identifiers
MONDO ID
MONDO_0021084
MESH ID
D014786
UMLS CUI
C0042790
MedGen ID
12103
SNOMED CT ID
128127008

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
CLN6 TTJCOQ7 moderate Biomarker [1]
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This Disease Is Related to 4 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
ATXN7 OTL3YF1H moderate Biomarker [2]
TSEN2 OT1UWYRI Definitive Biomarker [3]
TSEN34 OTH5FQHP Definitive Biomarker [3]
TSEN54 OT7MR9LY Definitive Biomarker [3]
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References

1 Altered biometal homeostasis is associated with CLN6 mRNA loss in mouse neuronal ceroid lipofuscinosis.Biol Open. 2013 May 20;2(6):635-46. doi: 10.1242/bio.20134804. Print 2013 Jun 15.
2 Clinical and molecular effect on offspring of a marriage of consanguineous spinocerebellar ataxia type 7 mutation carriers: a family case report.Int J Clin Exp Med. 2014 Dec 15;7(12):5896-903. eCollection 2014.
3 tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia. Nat Genet. 2008 Sep;40(9):1113-8. doi: 10.1038/ng.204.