Search Ontology:
Human Disease

factor V deficiency

Term ID
DOID:2216
Synonyms
  • deficiency, labile
  • Hereditary hypoproaccelerinaemia
  • Labile factor deficiency
  • Proaccelerin deficiency
Definition
References
  • GARD:2237
  • ICD10CM:D68.2
  • MESH:D005166
  • MIM:227400
  • NCI:C98938
  • SNOMEDCT_US_2023_03_01:191284007
  • UMLS_CUI:C0015499
Ontology
Human Disease   ( DOID:2216 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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