Disease #00462 (CDA (dystrophy, cornea, Avellino type (CDA)), OMIM:607541)
Official abbreviation |
CDA |
Name |
dystrophy, cornea, Avellino type (CDA) |
OMIM ID |
607541 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
8 |
Phenotype entries for this disease |
8 |
Associated with 1 gene |
TGFBI |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-07-21 14:34:39 +02:00 (CEST) |
Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|