thrombophilia, X-Linked, due to factor ix defect

Preferred Label : thrombophilia, X-Linked, due to factor ix defect;

Origin ID

C567581;

UMLS CUI

C2749016;

Automatic exact mappings (from CISMeF team)
- X-linked thrombophilia due to factor IX defect [DO Concept]
Currated CISMeF NLP mapping
- Thrombophilia, X-linked, due to factor ix defect [OMIM Phenotype]
DO Cross reference
- X-linked thrombophilia due to factor IX defect [DO Concept]
MeSH term(s) associated for indexing
- factor IX [MeSH Descriptor]
- genetic diseases, X-linked [MeSH Descriptor]
- thrombophilia [MeSH Descriptor]
Record concept(s)
- thrombophilia, X-Linked, due to factor ix defect [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Thrombophilia, X-linked, due to factor ix defect [OMIM Phenotype]
- X-linked thrombophilia due to factor IX defect [DO Concept]