prekallikrein deficiency

Preferred Label : prekallikrein deficiency;

MeSH note : mutation in KLKB1;

MeSH synonym : fletcher factor deficiency; PKK deficiency;

Origin ID

C562725;

UMLS CUI

C0272339;

Currated CISMeF NLP mapping
- Prekallikrein Deficiency [NCIt concept]
- Prekallikrein deficiency [OMIM Phenotype]
- Prekallikrein deficiency (disorder) [SNOMED CT concept]
- prekallikrein deficiency [SNOMED Notion]
MeSH term(s) associated for indexing
- blood coagulation disorders [MeSH Descriptor]
- prekallikrein [MeSH Descriptor]
Record concept(s)
- prekallikrein deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital prekallikrein deficiency [ORDO Disease]
- Prekallikrein Deficiency [NCIt concept]
- Prekallikrein deficiency [OMIM Phenotype]
- Prekallikrein deficiency (disorder) [SNOMED CT concept]
- prekallikrein deficiency [SNOMED Notion]