Disease #02055 (Revesz (Revesz syndrome), OMIM:268130)
Official abbreviation |
Revesz |
Name |
Revesz syndrome |
OMIM ID |
268130 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
2 |
Phenotype entries for this disease |
2 |
Associated with 1 gene |
TINF2 |
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
|