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
..expandKeratoconus (D007640)

       Child Nodes:
........expandKeratoconus 1 (C563649)
........expandKeratoconus 2 (C563827)
........expandKeratoconus 3 (C563900)
........expandKeratoconus 4 (C563752)
........expandKeratoconus And Congenital Hip Dysplasia (C565456)
........expandKeratoconus posticus circumscriptus (C536151)
........expandKeratoconus Posticus Circumscriptus with Associated Malformations (C565455)
........expandMental retardation, keratoconus, febrile seizures, and sinoatrial block (C537452)
........expandNoninflammatory corneal thinning (C531720)



 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:6054
Name:Keratoconus
Definition:A noninflammatory, usually bilateral protrusion of the cornea, the apex being displaced downward and nasally. It occurs most commonly in females at about puberty. The cause is unknown but hereditary factors may play a role. The -conus refers to the cone shape of the corneal protrusion. (From Dorland, 27th ed)
Alternative IDs:
ParentIDs:MESH:D003316
TreeNumbers:C11.204.627
Synonyms:
Slim Mappings:Eye disease
Reference: MedGen: D007640
MeSH: D007640
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants