Disease #02460 (Omenn (Omenn syndrome), OMIM:603554)
| Official abbreviation |
Omenn |
| Name |
Omenn syndrome |
| OMIM ID |
603554 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
20 |
| Phenotype entries for this disease |
2 |
| Associated with 3 genes |
DCLRE1C, RAG1, RAG2 |
| 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
|