OBO ID: DOID:2222
Term Name: factor X deficiency Search Ontology:
Synonyms:
  • disease, Stuart-Prower
Definition: A blood coagulation disease that is characterized by the partial or complete absence of factor X activity in the blood. https://rarediseases.org/rare-diseases/factor-x-deficiency/
References:
Ontology: Human Disease   ( DOID:2222 )
Relationships
is a type of:
OTHER factor X deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
F10 Factor X deficiency 227600
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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