# antithrombin III deficiency

> inherited blood coagulation disease characterized by the tendency to form clots in the veins

**Wikidata**: [Q3704732](https://www.wikidata.org/wiki/Q3704732)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Antithrombin_III_deficiency)  
**Source**: https://4ort.xyz/entity/antithrombin-iii-deficiency


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. UniProt
4. Antithrombin Oslo: type Ib classification of the first reported antithrombin-deficient family, with a review of hereditary antithrombin variants
5. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/dd6376b1-1593-461f-bfc8-cec5cfb1c3f8--2020-02-26T17:00:00)
6. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_dd6376b1-1593-461f-bfc8-cec5cfb1c3f8-2020-02-26T170000.000Z)
7. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000117601/MONDO_0013144)
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)
9. Human Phenotype Ontology release 2018-03-08
10. UMLS 2023
11. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)