UMLS CUI | C0272375 |
UMLS Term | Antithrombin Iii Deficiency |
MeSH ID | D020152 |
MeSH Term | Antithrombin III Deficiency |
Disease Classes |
Hemic and Lymphatic Diseases Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
Gene Symbol | Description | Entrez ID | Uniprot ID | Chromosomal Location |
---|---|---|---|---|
SERPINC1 |
serpin peptidase inhibitor, clade C (antithrombin), member 1 |
462 |
P01008 |
chr1: 173,903,804-173,917,378 |