Disease #02806 (Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive, OMIM:608971)
| Official abbreviation |
- |
| Name |
Severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive |
| OMIM ID |
608971 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 2 genes |
IL7R, PTPRC |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
N/A |
|
