heparin cofactor 2 deficiency

Summary

heparin cofactor 2 deficiency is a rare disease^[1].

Key Facts

• heparin cofactor 2 deficiency's instance of is recorded as rare disease^[2].
• heparin cofactor 2 deficiency's instance of is recorded as class of disease^[3].
• heparin cofactor 2 deficiency's subclass of is recorded as thrombophilia^[4].
• heparin cofactor 2 deficiency's subclass of is recorded as autosomal dominant disease^[5].
• heparin cofactor 2 deficiency's MeSH descriptor ID is recorded as C562865^[6].
• heparin cofactor 2 deficiency's OMIM ID is recorded as 612356^[7].
• heparin cofactor 2 deficiency's Disease Ontology ID is recorded as DOID:0111901^[8].
• heparin cofactor 2 deficiency's ICD-9-CM is recorded as 286.3^[9].
• heparin cofactor 2 deficiency's genetic association is recorded as SERPIND1^[10].
• heparin cofactor 2 deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111901^[11].
• heparin cofactor 2 deficiency's exact match is recorded as http://identifiers.org/doid/DOID:0111901^[12].
• heparin cofactor 2 deficiency's UMLS CUI is recorded as C0398626^[13].
• heparin cofactor 2 deficiency's Mondo ID is recorded as MONDO_0012876^[14].
• heparin cofactor 2 deficiency's ICD-11 ID is recorded as 1059796074^[15].
• heparin cofactor 2 deficiency's UniProt disease ID is recorded as DI-00541^[16].