Term info
database cross reference
- MESH:C538174 (MONDO:equivalentTo)
- NCIT:C131622 (MONDO:equivalentTo)
- Orphanet:26348 (MONDO:equivalentTo)
- GARD:0000475 (MONDO:equivalentTo)
- UMLS:C0392610 (Orphanet:26348)
- SCTID:4152002 (MONDO:equivalentTo)
Subsets
ordo_disease
definition
An instance of prothrombin deficiency that is acquired during the lifetime of the individual.
exactMatch
http://purl.obolibrary.org/obo/Orphanet_26348, http://identifiers.org/mesh/C538174, http://identifiers.org/snomedct/4152002, http://linkedlifedata.com/resource/umls/id/C0392610, http://purl.obolibrary.org/obo/NCIT_C131622
excluded subClassOf
http://purl.obolibrary.org/obo/MONDO_0013361
has exact synonym
acquired prothrombin deficiency, acquired hypoprothrombinemia
has related synonym
acquired factor II deficiency, hypoprothrombinemia, acquired
id
MONDO:0016990