Disease #00237 (ECTOL1 (ectopia lentis, type 1 (ECTOL-1)), OMIM:129600)
Official abbreviation |
ECTOL1 |
Name |
ectopia lentis, type 1 (ECTOL-1) |
OMIM ID |
129600 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
61 |
Phenotype entries for this disease |
55 |
Associated with 1 gene |
FBN1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2013-10-09 21:32:43 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|