Dysfibrinogenemia

Preferred Label : Dysfibrinogenemia;

Alternative definition : NICHD: A coagulation disorder caused by abnormalities in fibrin that result in defective clot formation. This disorder may be inherited or acquired.;

Details

Origin ID

C131659;

UMLS CUI

C1260903;

Automatic exact mappings (from CISMeF team)
- Dysfibrinogenemia [HPO term]
- Dysfibrinogenemia [PASCAL descriptor]
- Dysfibrinogenemia (disorder) [SNOMED CT concept]
Has associated anatomic sites
- Hematopoietic and Lymphatic System [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dysfibrinogenemia [PASCAL descriptor]
- Dysfibrinogenemia [HPO term]
- Dysfibrinogenemia (disorder) [SNOMED CT concept]
- dysfibrinogenemia [Disease (Nov.)]
- dysfibrinogenemia, nos [SNOMED Notion]
concept_is_in_subset
- NICHD Terminology [NCIt concept]
- Pediatric Hematology-Oncology Terminology [NCIt concept]
disease_has_normal_cell_origin
- Hematopoietic and Lymphoid Cell [NCIt concept]
disease_has_normal_tissue_origin
- Hematopoietic and Lymphoid Tissue [NCIt concept]
disease_has_primary_anatomic_site
- Hematopoietic and Lymphatic System [NCIt concept]

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