Disease Browser
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Parent Node: Pupil Disorders (D011681) | ..Starting node ..Ectopia pupillae (C536185)
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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
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM,ClinVar, CTD
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Term ID: | 4006 |
Name: | Ectopia pupillae |
Definition: | |
Alternative IDs: | OMIM:129750 |
ParentIDs: | MESH:D011681 |
TreeNumbers: | C10.597.690/C536185 |C11.710/C536185 |C23.888.592.708/C536185 |
Synonyms: | Familial ectopic pupil |
Slim Mappings: | Eye disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C536185
MeSH: C536185
OMIM: 129750; MSeqDR : Genes: | Phenotypes | | Disease Causing ClinVar Variants | | MSeqDR Portal | |
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