factor XIII, B subunit, deficiency of

Preferred Label : factor XIII, B subunit, deficiency of;

MeSH note : mutations in F13B;

Origin ID

C567688;

UMLS CUI

C2750481;

Automatic exact mappings (from CISMeF team)
- Factor XIII subunit B deficiency [HPO term]
Currated CISMeF NLP mapping
- Factor XIII, b subunit, deficiency of [OMIM Phenotype]
HPO term
- Factor XIII subunit B deficiency [HPO term]
MeSH term(s) associated for indexing
- factor xiii deficiency [MeSH Descriptor]
Record concept(s)
- factor XIII, B subunit, deficiency of [MeSH concept]
Semantic type(s)
- Finding [UMLS semantic type]
UMLS correspondences (same concept)
- Factor XIII subunit B deficiency [HPO term]
- Factor XIII, b subunit, deficiency of [OMIM Phenotype]