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 |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|