Disease #04209 (RPad (retinitis pigmentosa, autosomal dominant (RPad)))
Official abbreviation |
RPad |
Name |
retinitis pigmentosa, autosomal dominant (RPad) |
OMIM ID |
- |
Inheritance |
- |
Individuals reported having this disease |
139 |
Phenotype entries for this disease |
139 |
Associated with 0 genes |
- |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2015-02-27 18:53:37 +01:00 (CET) |
Date last edited |
N/A |
Individuals
|
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