General Information of Disease (ID: DISRWZEG)

Disease Name Retinitis
Synonyms retina inflammation; inflammation of retina
Definition Inflammation of the retina.
Disease Hierarchy
DISWD40R: Disease
DISB4B0F: Retinopathy
DISIBJSM: Posterior uveitis
DISRWZEG: Retinitis
Disease Identifiers
MONDO ID
MONDO_0002708
MESH ID
D012173
UMLS CUI
C0035333
MedGen ID
19765
HPO ID
HP:0032118
SNOMED CT ID
399463004

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 3 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
CRH TTA7YIZ Strong Biomarker [1]
MIF TT6804T Strong Biomarker [2]
PRKCG TTRFOXJ Strong Genetic Variation [3]
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This Disease Is Related to 1 DTP Molecule(s)
Gene Name DTP ID Evidence Level Mode of Inheritance REF
SLC9A6 DTN0JXW Strong Genetic Variation [4]
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This Disease Is Related to 3 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DPYSL5 OT6F9T6F Strong Biomarker [5]
NDP OTGDJ4US Strong Biomarker [6]
RLBP1 OTCY4D6B Strong Genetic Variation [7]
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References

1 Fas/Fas ligand-associated apoptosis in experimental autoimmune uveoretinitis in rodents: role of proinflammatory corticotropin-releasing hormone.Exp Eye Res. 2001 Jun;72(6):623-9. doi: 10.1006/exer.2001.0992.
2 Inhibition of experimental autoimmune uveoretinitis with anti-macrophage migration inhibitory factor antibodies.Curr Eye Res. 2000 Feb;20(2):109-14.
3 R659S mutation of gammaPKC is susceptible to cell death: implication of this mutation/polymorphism in the pathogenesis of retinitis pigmentosa.Neurochem Int. 2006 Dec;49(7):669-75. doi: 10.1016/j.neuint.2006.05.005. Epub 2006 Jul 7.
4 Novel mutation in SLC9A6 gene in a patient with Christianson syndrome and retinitis pigmentosum.Brain Dev. 2013 Feb;35(2):172-6. doi: 10.1016/j.braindev.2012.03.010. Epub 2012 Apr 26.
5 Paraneoplastic autoimmune optic neuritis with retinitis defined by CRMP-5-IgG.Ann Neurol. 2003 Jul;54(1):38-50. doi: 10.1002/ana.10587.
6 Cystoid edema, neovascularization and inflammatory processes in the murine Norrin-deficient retina.Sci Rep. 2018 Apr 13;8(1):5970. doi: 10.1038/s41598-018-24476-y.
7 Novel mutation in RLBP1 gene in a Japanese patient with retinitis punctata albescens.Am J Ophthalmol. 2005 Jun;139(6):1133-5. doi: 10.1016/j.ajo.2004.12.011.