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Antithrombin Iii Deficiency

Disease ID: disease_node_10120

Connections displayed (default: 10).

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Dbxref	ICD10CM:D68.59, MESH:D020152, MIM:613118, NCI:C98815, SNOMEDCT_US_2023_03_01:36351005, UMLS_CUI:C0272375
Subclassof	DOID_2452, DOID_0050736, DOID_0050737
Data Source	DOID, MESH
Synonyms	AT III deficiency, hereditary thrombophilia due to congenital antithrombin deficiency
Mesh Id	D020152
Mesh Label	Antithrombin III Deficiency
Mesh Subclassof	D025861, D001796, D019851
Doid Label	antithrombin III deficiency
Doid Description	A thrombophilia that is characterized by the tendency to form clots in the veins. Xref MGI.
Has Material Basis In	GENO_0000147, GENO_0000148
Disease Node Id	disease_node_10120
Doid Id	DOID_3755
Label	Antithrombin Iii Deficiency

Outgoing r'ship SUBCLASS_OF to/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)
Outgoing r'ship SUBCLASS_OF to/from Thrombophilia(ID:disease_node_10025) (Disease)

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