Jump to:
loading...| Preferred Name | X-Linked Severe Combined Immunodeficiency | |
| Synonyms |
|
|
| Definitions |
Rare congenital disorder inherited as an X-linked defect characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. |
|
| ID |
http://purl.obolibrary.org/obo/NCIT_C4682 |
|
| code |
C4682 |
|
| Contributing_Source |
Cellosaurus |
|
| definition |
Rare congenital disorder inherited as an X-linked defect characterized by impairment of both humoral and cell-mediated immunity, leukopenia, and low or absent antibody levels. |
|
| in_subset | ||
| label |
X-Linked Severe Combined Immunodeficiency |
|
| Legacy Concept Name |
X-Linked_Severe_Combined_Immunodeficiency |
|
| Preferred_Name |
X-Linked Severe Combined Immunodeficiency |
|
| prefixIRI |
NCIT:C4682 |
|
| prefLabel |
X-Linked Severe Combined Immunodeficiency |
|
| Semantic_Type |
Disease or Syndrome |
|
| UMLS_CUI |
C1279481 |
|
| subClassOf |
Create mapping