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
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