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[X] prekallikrein deficiency

Go to external page http://purl.obolibrary.org/obo/MONDO_0044744

A condition characterized by the congenital or acquired deficiency of prekallikrein. This deficiency is usually not associated with bleeding. The congenital deficiency is very rare. Acquired deficiency may occur in diffuse intravascular coagulation, infections, and sickle cell disease. [ NCIT:C99022 ]

Synonyms: prekallikrein deficiency

This is just here as a test because I lose it

Term information

database cross reference
  • NCIT:C99022 (MONDO:equivalentTo)
  • UMLS:C0272339 (MONDO:equivalentTo)
  • MEDGEN:75779 (MONDO:equivalentTo)
  • SCTID:48976006 (MONDO:equivalentTo)
  • NANDO:2200684 (https://orcid.org/0000-0003-0011-764X)
Subsets

matrix_llm__is_cancer_other, gard_rare, matrix_llm__is_glucose_dysfunction_other, otar, matrix_excluded, matrix_llm__tag_qualy_lost_other, mondo_top_grouping_hematologic_disorder, matrix_llm__txgnn_other, mondo_top_grouping_member, matrix_llm__medical_specialization_other, matrix_llm__tag_existing_treatment_other, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, harrisons_view_hematologic_disorder, rare, harrisons_view_member

exactMatch

http://purl.obolibrary.org/obo/NCIT_C99022

http://linkedlifedata.com/resource/umls/id/C0272339

http://identifiers.org/medgen/75779

http://identifiers.org/snomedct/48976006

id

MONDO:0044744

Term relations