Disease #00988 (RSSCID (immunodeficiency, severe combined, Athabascan type), OMIM:602450)
| Official abbreviation |
RSSCID |
| Name |
immunodeficiency, severe combined, Athabascan type |
| OMIM ID |
602450 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
2 |
| Associated with 2 genes |
DCLRE1C, LIG4 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2021-12-11 13:56:28 +01:00 (CET) |
Individuals
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