Disease #07034 (IMD105 (immunodeficiency, type 105, severe combined), OMIM:619924)
| Official abbreviation |
IMD105 |
| Name |
immunodeficiency, type 105, severe combined |
| OMIM ID |
619924 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
PTPRC |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2023-10-17 16:07:11 +02:00 (CEST) |
| Date last edited |
N/A |
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