OBO ID: DOID:2231
Term Name: factor XII deficiency Search Ontology:
Synonyms:
  • deficiency, Hageman
  • Factor XII deficiency disease
  • Hageman Factor deficiency
Definition: A blood coagulation disease that is characterized by prolonged PTT time without clinical symptoms, and has_material_basis_in a mutation in the F12 gene on chromosome 5q33. (2)
References:
Ontology: Human Disease   ( DOID:2231 )
Relationships
is a type of:
OTHER factor XII deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F12 Factor XII deficiency
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.