Disease Description

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