Disease #07117 (PERRS2 (prolonged electroretinal response suppression, type 2), OMIM:620344)
Official abbreviation |
PERRS2 |
Name |
prolonged electroretinal response suppression, type 2 |
OMIM ID |
620344 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
RGS9BP |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2024-11-11 21:43:12 +01:00 (CET) |
Date last edited |
N/A |
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