Disease #01338 (FECD1 (dystrophy, corneal, Fuchs endothelial, type 1 (FECD-1)), OMIM:136800)
| Official abbreviation |
FECD1 |
| Name |
dystrophy, corneal, Fuchs endothelial, type 1 (FECD-1) |
| OMIM ID |
136800 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
19 |
| Phenotype entries for this disease |
6 |
| Associated with 1 gene |
COL8A2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|