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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
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Macular Degeneration (D008268)
..Starting node
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Macular Edema (D008269)

       Child Nodes:



 Sister Nodes: 
..expandEctodermal dysplasia, ectrodactyly, and macular dystrophy (C536190)
..expandFundus Dystrophy, Pseudoinflammatory, Of Sorsby (C564992)
..expandGeographic Atrophy (D057092)
..expandJuvenile macular degeneration and hypotrichosis (C537698)
..expandMacular Degeneration, Age-Related, 1 (C566411)
..expandMacular Degeneration, Age-Related, 10 (C566935)
..expandMacular Degeneration, Age-Related, 11 (C567450)
..expandMacular Degeneration, Age-Related, 2 (C562479)
..expandMacular Degeneration, Age-Related, 3 (C563838)
..expandMacular Degeneration, Age-Related, 4 (C565196)
..expandMacular Degeneration, Age-Related, 6 (C563674)
..expandMacular Degeneration, Age-Related, 7 (C565718)
..expandMacular Degeneration, Age-Related, 9 (C566958)
..expandMacular dystrophy, concentric annular (C537833)
..expandMACULAR DYSTROPHY, RETINAL, 3 (OMIM:608850)
..expandMacular Dystrophy, X-Linked (C564110)
..expandMacular Edema (D008269)
..expandMyoclonic Epilepsy, Congenital Deafness, Macular Dystrophy, and Psychiatric Disorders (C565786)
..expandOCCULT MACULAR DYSTROPHY (OMIM:613587)
..expandStargardt disease 1 (C535804)
..expandStargardt disease 3 (C535805)
..expandStargardt disease 4 (C535521)
..expandStargardt Macular Degeneration (C580470)
..expandStargardt Macular Degeneration Absent or Hypoplastic Corpus Callosum Mental Retardation and Dysmorphic Features (C548086)
..expandVitelliform Macular Dystrophy (D057826) Child2
..expandWet Macular Degeneration (D057135)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:6695
Name:Macular Edema
Definition:Fluid accumulation in the outer layer of the MACULA LUTEA that results from intraocular or systemic insults. It may develop in a diffuse pattern where the macula appears thickened or it may acquire the characteristic petaloid appearance referred to as cystoid macular edema. Although macular edema may be associated with various underlying conditions, it is most commonly seen following intraocular surgery, venous occlusive disease, DIABETIC RETINOPATHY, and posterior segment inflammatory disease. (From Survey of Ophthalmology 2004; 49(5) 470-90)
Alternative IDs:OMIM:153880
ParentIDs:MESH:D008268
TreeNumbers:C11.768.585.439.245
Synonyms:Central Retinal Edema, Cystoid |CYMD |Cystoid Macular Dystrophy |Cystoid Macular Edema |Cystoid Macular Edema, Postoperative |DCMD |Edema, Cystoid Macular |Edema, Macular |Irvine Gass Syndrome |Irvine-Gass Syndrome |Macular Dystrophy, Dominant Cystoid |Macular Edem
Slim Mappings:Eye disease
Reference: MedGen: D008269
MeSH: D008269
OMIM: 153880;

Genes: CYMD;
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0011505Cystoid macular edema
3 HP:0000969Edema
4 HP:0000540Hypermetropia
5 HP:0007754Macular dystrophy
6 HP:0007947Pericentral retinitis pigmentosa
7 HP:0000486Strabismus
Disease Causing ClinVar Variants