Disease #02363 (SCIDN (immunodeficiency, severe combined, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive), OMIM:601457)
| Official abbreviation |
SCIDN |
| Name |
immunodeficiency, severe combined, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive |
| OMIM ID |
601457 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
8 |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
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
|