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congenital afibrinogenemia

^ http://purl.obolibrary.org/obo/MONDO_0008737

Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen. [ Orphanet:98880 ]

Term info

database cross reference
  • SCTID:154818001 (MONDO:equivalentTo)
  • NCIT:C98130 (MONDO:equivalentTo)
  • Orphanet:98880 (OMIM:202400)
  • DOID:2236 (MONDO:equivalentTo)
  • GARD:0005761 (MONDO:equivalentTo)
  • MESH:D000347 (MONDO:equivalentTo)
  • OMIM:202400 (Orphanet:98880/e)
Subsets

ordo_clinical_subtype

definition

Familial afibrinogenemia is a coagulation disorder characterized by bleeding symptoms due to a complete absence of circulating fibrinogen.

exactMatch

http://purl.obolibrary.org/obo/DOID_2236, http://identifiers.org/snomedct/154818001, http://purl.obolibrary.org/obo/Orphanet_98880, http://purl.obolibrary.org/obo/NCIT_C98130, https://omim.org/entry/202400, http://identifiers.org/mesh/D000347

has exact synonym

fibrinogen deficiency

has narrow synonym

factor I deficiency

has related synonym

afibrinogenemia, hypofibrinogenemia, congenital, afibrinogenemia congenital, afibrinogenemia, congenital, familial afibrinogenemia

id

MONDO:0008737

Term relations