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congenital factor X deficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0009212

Congenital factor X deficiency is an inherited bleeding disorder with a decreased antigen and/or activity of factor X (FX) and characterized by mild to severe bleeding symptoms. [ Orphanet:328 ]

Synonyms: congenital Stuart factor deficiency congenital factor X deficiency disease, Stuart-Prower Stuart-Prower factor deficiency hereditary Factor X deficiency

This is just here as a test because I lose it

Term information

database cross reference
  • ICD9:286.3 (MONDO:relatedTo)
  • DOID:2222 (MONDO:equivalentTo)
  • NCIT:C98940 (MONDO:equivalentTo)
  • OMIM:227600 (Orphanet:328/e)
  • Orphanet:328 (OMIM:227600)
  • SCTID:37350004 (https://github.com/monarch-initiative/mondo/issues/2944)
  • GARD:6404 (Orphanet:328)
Subsets

gard_rare, ordo_disease, rare, nord_rare, orphanet_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/4069

exactMatch

http://purl.obolibrary.org/obo/DOID_2222

http://www.orpha.net/ORDO/Orphanet_328

http://identifiers.org/snomedct/37350004

http://purl.obolibrary.org/obo/NCIT_C98940

https://omim.org/entry/227600

has related synonym

factor X deficiency, congenital

Stuart-Prower Factor deficiency

Stuart factor deficiency, congenital

factor 10 deficiency

factor X deficiency

F10 deficiency

id

MONDO:0009212

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0009212