Disease #05899 (RENS1 (Renpenning syndrome, type 1 (RENS1)), OMIM:309500)
| Official abbreviation |
RENS1 |
| Name |
Renpenning syndrome, type 1 (RENS1) |
| OMIM ID |
309500 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
X-linked recessive |
| Individuals reported having this disease |
1 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
PQBP1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2021-02-09 15:16:23 +01:00 (CET) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|