Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandCorneal Diseases (D003316)
..Starting node
..expandCorneal Opacity (D003318)

       Child Nodes:
........expandArcus Senilis (D001112)
........expandAXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
........expandDe Barsy syndrome (C535990)
........expandKyrle disease (C538130)
........expandMental retardation Mietens Weber type (C537444)
........expandMicrophthalmia and mental deficiency (C537462)
........expandPeters anomaly (C537884)
........expandRosenthal-Kloepfer syndrome (C535654)
........expandSpondyloepiphyseal dysplasia tarda, Toledo type (C535787)
........expandWinchester syndrome (C536709)



 Sister Nodes: 
..expandArnold Stickler Bourne syndrome (C537431)
..expandCataract microcornea syndrome (C538287)
..expandCornea Plana 1 (C565158)
..expandCornea Plana 2 (C565677)
..expandCorneal Dystrophies, Hereditary (D003317) Child61
..expandCorneal Edema (D015715)
..expandCorneal Endothelial Cell Loss (D055954)
..expandCorneal hypesthesia, familial (C536440)
..expandCorneal Injuries (D065306) Child1
..expandCorneal Neovascularization (D016510)
..expandCorneal Opacity (D003318) Child10
..expandCorneal Wavefront Aberration (D057108)
..expandDermoids of cornea (C535376)
..expandIridocorneal Endothelial Syndrome (D057129)
..expandKeratitis (D007634) Child14
..expandKeratoconus (D007640) Child9
..expandMacrophthalmia, Colobomatous, with Microcornea (C566533)
..expandMicrospherophakia (C563255)
..expandNeuhauser syndrome (C536143)
..expandRamos Arroyo Clark syndrome (C535286)
..expandRing dermoid of cornea (C535684)
..expandSclerocornea (C565209)
..expandSclerocornea, Autosomal Dominant (C566692)
..expandStern Lubinsky Durrie syndrome (C537488)
..expandTrachoma (D014141)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2746
Name:Corneal Opacity
Definition:Disorder occurring in the central or peripheral area of the cornea. The usual degree of transparency becomes relatively opaque.
Alternative IDs:
ParentIDs:MESH:D003316
TreeNumbers:C11.204.299
Synonyms:Corneal Opacities |Leukoma |Leukomas |Opacities, Corneal |Opacity, Corneal
Slim Mappings:Eye disease
Reference: MedGen: D003318
MeSH: D003318
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants