Disease #02825 (PPCD3 (dystrophy, corneal, posterior polymorphous, type 3 (PPCD-3)), OMIM:609141)
Official abbreviation |
PPCD3 |
Name |
dystrophy, corneal, posterior polymorphous, type 3 (PPCD-3) |
OMIM ID |
609141 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
3 |
Phenotype entries for this disease |
3 |
Associated with 1 gene |
ZEB1 |
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
|