ZFIN Human Disease: antithrombin III deficiency

OBO ID: DOID:3755

Term Name:	antithrombin III deficiency		Search Ontology:
Synonyms:	AT III deficiency hereditary thrombophilia due to congenital antithrombin deficiency
Definition:	A thrombophilia that is characterized by the tendency to form clots in the veins. (2)
References:	ICD10CM:D68.59 MESH:D020152 NCI:C98815 OMIM:613118 SNOMEDCT_US_2023_03_01:36351005 UMLS_CUI:C0272375
Ontology:	Human Disease ( DOID:3755 )

Relationships

is a type of:	autosomal dominant disease autosomal recessive disease thrombophilia autosomal dominant disease autosomal recessive disease thrombophilia Show first 5 Terms

OTHER antithrombin III deficiency PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
SERPINC1	serpinc1	Thrombophilia 7 due to antithrombin III deficiency	613118

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None