Disease Browser
|
Parent Node: Corneal Dystrophies, Hereditary (D003317) | Parent Node: Pupil Disorders (D011681) | ..Starting node ..Congenital Corneal Opacities, Cornea Guttata, and Corectopia (C563921)
| Child Nodes:
|
Sister Nodes: | ..Anisocoria (D015875)
| ..Congenital Corneal Opacities, Cornea Guttata, and Corectopia (C563921)
| ..Ectopia Lentis with Ectopia of Pupil (C563268)
| ..Ectopia pupillae (C536185)
| ..McPherson Robertson Cammarano syndrome (C538161)
| ..Microcoria, congenital (C537550)
| ..Microphthalmia, Isolated, With Corectopia (C563581)
| ..Miosis (D015877) 5
| ..Mydriasis (D015878) 1
| ..Pierson syndrome (C537185)
| ..Ptosis, Strabismus, And Ectopic Pupils (C566736)
| ..Tonic Pupil (D015845) 2
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
|
|
|
Term ID: | 2884 |
Name: | Congenital Corneal Opacities, Cornea Guttata, and Corectopia |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D003317|MESH:D011681 |
TreeNumbers: | C10.597.690/C563921 |C11.204.236/C563921 |C11.270.162/C563921 |C11.710/C563921 |C16.320.290.162/C563921 |C23.888.592.708/C563921 |
Synonyms: | Corneal Opacities, Congenital, with Cornea Guttata and Corectopia |
Slim Mappings: | Eye disease|Genetic disease (inborn)|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C563921
MeSH: C563921
OMIM: MSeqDR : Genes: CD96; | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
|