Disease #00465 (CDL3A (dystrophy, corneal, lattice type IIIA (CDL-3A)), OMIM:608471)
| Official abbreviation |
CDL3A |
| Name |
dystrophy, corneal, lattice type IIIA (CDL-3A) |
| OMIM ID |
608471 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal dominant |
| Individuals reported having this disease |
18 |
| Phenotype entries for this disease |
18 |
| Associated with 1 gene |
TGFBI |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-07-21 14:41:21 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
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