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
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