Disease #05842 (RRS1 (Robinow, autosomal recessive syndrome, type 1 (RRS1)), OMIM:268310)
| Official abbreviation |
RRS1 |
| Name |
Robinow, autosomal recessive syndrome, type 1 (RRS1) |
| OMIM ID |
268310 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
1 |
| Associated with 1 gene |
ROR2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2020-09-29 10:02:52 +02:00 (CEST) |
| Date last edited |
2021-12-10 21:51:32 +01:00 (CET) |
Individuals
|