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:
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Eye Diseases (D005128)
..Starting node
..expand
Corneal Diseases (D003316)

       Child 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)



 Sister Nodes: 
..expandAsthenopia (D001248)
..expandCogan Syndrome (D055952) Child2
..expandConjunctival Diseases (D003229) Child29
..expandCorneal Diseases (D003316) Child120
..expandEncephalocraniocutaneous lipomatosis (C535736)
..expandExudative Vitreoretinopathy 4 (C566619)
..expandExudative Vitreoretinopathy 5 (C567648)
..expandEye Abnormalities (D005124) Child208
..expandEye Diseases, Hereditary (D015785) Child373
..expandEye Hemorrhage (D005130) Child6
..expandEye Infections (D015817) Child25
..expandEye Injuries (D005131) Child7
..expandEye Manifestations (D005132) Child9
..expandEye Neoplasms (D005134) Child20
..expandEyelid Diseases (D005141) Child64
..expandHernandez Fragoso syndrome (C536062)
..expandLacrimal Apparatus Diseases (D007766) Child18
..expandLens Diseases (D007905) Child166
..expandMollica Pavone Antener syndrome (C535809)
..expandMORM syndrome (C536984)
..expandNeuropathy, Hereditary Sensorimotor, with Upper Motor Neuron, Visual Pathway and Autonomic Disturbance (C563517)
..expandOcular Hypertension (D009798) Child52
..expandOcular Hypotension (D015814)
..expandOcular Motility Disorders (D015835) Child109
..expandOptic Nerve Diseases (D009901) Child69
..expandOrbital Diseases (D009916) Child17
..expandPupil Disorders (D011681) Child20
..expandRefractive Errors (D012030) Child57
..expandRetinal Diseases (D012164) Child287
..expandScleral Diseases (D015422) Child3
..expandUveal Diseases (D014603) Child59
..expandVision Disorders (D014786) Child84
..expandVitreoretinopathy, Proliferative (D018630) Child5
..expandVitreous Detachment (D020255) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:2709
Name:Corneal Diseases
Definition:Diseases of the cornea.
Alternative IDs:
ParentIDs:MESH:D005128
TreeNumbers:C11.204
Synonyms:Corneal Disease |Disease, Corneal |Diseases, Corneal
Slim Mappings:Eye disease
Reference: MedGen: D003316
MeSH: D003316
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants