FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term antithrombin III deficiency ID (Ontology) DOID:3755 (Human Disease)
Definition A thrombophilia that is characterized by the tendency to form clots in the veins.
Also Known As "AT III deficiency" ; "hereditary thrombophilia due to congenital antithrombin deficiency"
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 Genes
 antithrombin III deficiency       5
 for disease ribbon | antithrombin III deficiency       5
 model of | antithrombin III deficiency       5
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease___
 |__autosomal recessive disease__|
blood coagulation disease        |
 |__thrombophilia________________|
                                 antithrombin III deficiency  5 rec.
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Is a autosomal dominant disease
autosomal recessive disease
thrombophilia
Part of
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Synonyms
  • "AT III deficiency" EXACT
    "hereditary thrombophilia due to congenital antithrombin deficiency" EXACT
Secondary IDs
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ICD10CM:D68.59
MESH:D020152
MIM:613118
NCI:C98815
SNOMEDCT_US_2023_03_01:36351005
UMLS_CUI:C0272375